HSQY 11-layer PA/PE easy-peel medical packaging film combines PA toughness with PE sealing performance. Available in 30-450μm thicknesses and 200-4000mm widths for medical devices and textiles.
HSQY
Flexible Packaging Films
Clear
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PA/PE Co-extrusion Film
HSQY 11-layer PA/PE co-extrusion film is a clear, printable multilayer flexible packaging film positioned for medical device and medical textile packaging projects requiring mechanical protection, puncture resistance, heat sealing and controlled easy-peel opening.
The current product specification lists a PA + PE material system, thicknesses from 0.03mm to 0.45mm and roll widths from 200mm to 4000mm. PA contributes mechanical toughness and puncture resistance, while PE supports flexibility, moisture resistance and heat-sealing performance.
This product is marketed as an easy-peel medical packaging film. Actual peel force, seal strength and opening behavior depend on the exact film grade, opposite sealing substrate, seal temperature, pressure and dwell time. The finished packaging system should therefore be evaluated under the customer's actual packaging and sterilization conditions.
PA/PE Medical Packaging Film
Clear Printable Co-Extrusion Film
Multilayer Medical Packaging Film
| Property | Specification |
|---|---|
| Product Name | 11-Layer PA/PE Easy-Peel Medical Packaging Film |
| Film Type | Multilayer Co-Extrusion Film |
| Number of Layers | 11 Layers according to current product positioning; exact layer sequence should be confirmed from the selected grade specification |
| Material | PA + PE |
| Appearance | Clear |
| Printing | Printable option listed in current product specification |
| Width | 200-4000mm |
| Thickness | 0.03-0.45mm / approximately 30-450μm |
| Opening Function | Easy-Peel product positioning; actual peel performance depends on sealing partner and process parameters |
| Primary Application | Medical Device and Medical Textile Packaging |
| Seal Function | Heat-sealing capability; exact sealing substrate and seal window should be confirmed |
Important: The current HSQY source does not publish the exact 11-layer sequence, OTR, WVTR, peel force, seal strength, sealing window, sterilization compatibility, roll core diameter, maximum roll OD or medical packaging validation data. These values should be obtained for the exact film grade before it is specified for a validated medical packaging system.
PA and PE provide different functions within a multilayer co-extruded structure. The exact layer arrangement can vary according to the required film grade, so the final construction should be confirmed through the applicable technical data sheet.
| Material | Typical Role in the Film |
|---|---|
| PA / Polyamide / Nylon | Mechanical strength, toughness, flex resistance and puncture resistance, with gas-barrier contribution according to the final structure |
| PE / Polyethylene | Flexibility, moisture resistance and heat-sealing functionality according to the selected sealing layer |
A multilayer co-extrusion process allows different polymer layers to perform different mechanical, barrier, sealing and processing functions within one flexible film.
For medical packaging, this can allow the film designer to balance puncture resistance, flexibility, sealability, transparency and converting performance according to the medical product and packaging equipment.
The phrase “11-layer” should not be used to infer a specific layer sequence unless that sequence is confirmed for the supplied film grade. Buyers requiring a defined construction should request the complete layer structure and material declaration.
Easy peel in medical packaging should provide controlled opening without making the package seal unnecessarily weak during production, distribution or storage.
Actual peel behavior is created by the complete seal interface. Film formulation, opposite sealing substrate, seal temperature, pressure, dwell time and package geometry can all influence peel force and opening quality.
Medical packaging buyers should therefore specify whether they require easy peel, controlled peel or another opening characteristic and provide the exact substrate to which the film will be sealed.
| Parameter | Why It Matters |
|---|---|
| Seal Strength | The package needs sufficient seal integrity for the intended processing, handling, distribution and storage conditions. |
| Peel Force | Opening force should match the intended package design and method of product presentation. |
| Clean Peel | The finished seal interface should be evaluated for undesirable tearing, delamination, stringing or fiber transfer where relevant. |
| Seal Window | Stable sealing performance should be established across the actual temperature, pressure and dwell-time range used on the packaging machine. |
The current HSQY product is positioned for medical device packaging projects requiring a clear multilayer flexible film with mechanical protection and heat-sealing capability.
Device geometry is particularly important when selecting thickness. Rigid edges, corners or projecting components can create greater puncture and flex stress than soft products, so film gauge should be evaluated against the actual packaged device.
Medical textiles are specifically identified in the current product positioning. Suitable film grades can be evaluated for textile-based healthcare products where clear visibility, flexible packaging and controlled sealing are required.
The textile material, package dimensions, sterilization method, required barrier performance and opening procedure should all be provided when selecting the film.
The current specification lists the PA/PE film as clear, allowing packaged components to remain visible through the flexible web.
For projects requiring defined optical performance, buyers should request haze and light-transmission data for the exact thickness and grade rather than relying only on a general “high transparency” description.
Printable film is included in the current HSQY specification. Printing can be used for identification, instructions, branding and other packaging information according to the selected converting system.
Buyers should provide the required printing process, number of colors, treatment requirement and ink system. Where sterilization is involved, printing and ink performance should also be evaluated after the intended sterilization cycle.
PA contributes toughness and puncture resistance to multilayer packaging film, helping the package withstand mechanical stresses generated during converting, handling and distribution.
The current product information does not publish puncture-force, tensile-strength, elongation or dart-impact values. Projects with defined mechanical requirements should request test data for the exact film thickness and construction.
The original HSQY description references barrier protection against oxygen and moisture. Exact barrier performance, however, depends on the complete multilayer construction, thickness and test conditions.
This page does not publish OTR or WVTR values. Buyers with defined oxygen- or moisture-barrier requirements should provide target values and test conditions when requesting a film recommendation.
Where substantially higher oxygen-barrier performance is required, an EVOH-containing medical packaging structure may be more appropriate than a standard PA/PE film and should be evaluated separately.
| Selection Factor | PA/PE Medical Film | PA/PP/EVOH/PE High-Barrier Film |
|---|---|---|
| Primary Positioning | Mechanical protection, flexibility, PE sealing and easy-peel medical packaging projects | Applications requiring enhanced oxygen-barrier performance from an EVOH-containing structure |
| Barrier Layer | No EVOH layer is identified in the current PA/PE product specification | EVOH is used as the principal enhanced oxygen-barrier component |
| Selection Basis | Peel, seal, puncture, flexibility and project-specific barrier requirements | Target OTR together with mechanical, sealing and sterilization requirements |
Peel behavior cannot be selected from the PA/PE film alone. Buyers should identify the exact substrate that will be sealed to the film, such as a specified medical paper, nonwoven lidding material, polymer film or other packaging web.
Compatibility should be confirmed using the actual mating substrate. Do not assume that one easy-peel PA/PE grade will provide identical peel behavior against every coated paper, nonwoven or plastic web.
The supplied HSQY source does not state which sterilization processes this exact PA/PE grade has been qualified for.
Medical packaging materials can respond differently to ethylene oxide, radiation, steam, plasma and other sterilization processes. Buyers should provide the intended sterilization method and processing conditions before selecting the film.
Seal integrity, material appearance, mechanical performance and peel behavior should be evaluated before and after the intended sterilization cycle as part of the complete packaging-system qualification.
A medical packaging film is one component of the finished packaging system. Suitability depends on the packaged device, mating substrate, sealing process, sterilization cycle, distribution conditions and required shelf life.
For terminally sterilized medical devices, customers should evaluate the complete packaging system against the applicable medical packaging and regulatory requirements for their market, including relevant ISO 11607 requirements where applicable.
A general company quality certificate should not be treated as evidence that every PA/PE film configuration is approved as a sterile barrier system.
| Selection Parameter | Information to Confirm |
|---|---|
| Medical Product | Device or medical textile type, dimensions, weight and geometry |
| Film Thickness | 30-450μm according to mechanical protection and package requirements |
| Roll Width | 200-4000mm according to packaging equipment and finished package dimensions |
| Sealing Substrate | Exact paper, nonwoven, film or other material sealed to the PA/PE web |
| Peel Requirement | Easy peel, controlled peel, target peel force or other opening requirement |
| Barrier Requirement | Target OTR, WVTR or other environmental protection requirement where applicable |
| Sterilization | Required sterilization method and cycle conditions |
| Packaging Equipment | Machine type, sealing system, operating speed and roll requirements |
| Printing | Printing process, colors, treatment and ink compatibility requirements |
| Technical Documentation | Required specifications, test reports and destination-market documentation |
Exact 11-layer film structure
Individual polymer and tie-layer configuration
Total film thickness and tolerance
Roll width and width tolerance
Core diameter and maximum roll outer diameter
OTR and test conditions where oxygen barrier is required
WVTR and test conditions where moisture barrier is required
Seal initiation temperature and operating seal window
Seal strength
Easy-peel force and peel consistency
Puncture and tensile properties
Haze and optical properties where required
Sterilization compatibility for the exact grade
Printing treatment and ink compatibility
Applicable medical packaging or regulatory documentation
| Requirement | Information to Provide |
|---|---|
| Product Type | Medical device, medical textile or other healthcare product |
| Film Thickness | Required μm or mm |
| Roll Width | Required width in mm |
| Peel Requirement | Easy peel, controlled peel or target peel-force requirement |
| Mating Substrate | Medical paper, nonwoven, film or other sealing material |
| Sterilization Method | Provide the intended method and processing conditions if sterilization is required |
| Barrier Target | OTR, WVTR or other barrier requirement where applicable |
| Packaging Machine | Machine type, brand/model and sealing process where available |
| Printing | Printable or unprinted, number of colors and printing process |
| Documentation | Required test reports, quality documents and market-specific requirements |
| Quantity | Trial quantity and expected recurring consumption |
| Destination | Country and destination port |
Medical Packaging Film Roll
Flexible Film Production
Film Roll Packing
Sample Packaging: Small rolls packed in protective boxes.
Bulk Packing: Rolls wrapped in PE film or kraft paper.
Pallet Packing: 500-2000kg per plywood pallet for secure transport.
Container Loading: Current product information lists approximately 20 tons per container.
Delivery Terms: EXW, FOB, CNF, DDU.
Lead Time: Generally 10-14 working days according to the current product information, depending on specification and order quantity.
HSQY displays certification documentation with this product. Medical packaging buyers should confirm which certificates and technical reports apply to the exact PA/PE film grade being purchased. General company certificates should not be interpreted as medical sterile-barrier approval for every film construction.
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2018 Shanghai Exhibition
2023 American Exhibition
It is a multilayer co-extruded flexible film using PA and PE materials to combine mechanical protection, flexibility, moisture resistance and heat-sealing functionality for suitable medical packaging applications.
The current product source identifies the film as 11-layer PA/PE but does not publish the complete individual layer sequence. Request the current technical specification for the exact film grade.
PA contributes toughness, mechanical strength, flex resistance and puncture resistance and can also contribute gas-barrier performance according to the overall structure.
PE can provide flexibility, moisture resistance and heat-sealing functionality in a multilayer film, depending on the specific PE grade and layer arrangement.
No. The technical table for this product identifies the material as PA + PE. PA/PP is a different material combination and should be treated as a separate medical packaging film structure.
The current specification lists 0.03-0.45mm, approximately 30-450μm.
The current HSQY specification lists widths from 200mm to 4000mm.
The product is positioned as an easy-peel medical packaging film. Actual peel force and clean-opening behavior depend on the selected film grade, mating substrate and sealing process.
Compatibility depends on the exact PE sealing layer and the coating or surface of the medical paper. Provide the exact paper specification and conduct seal-strength and peel testing before commercial use.
Potential compatibility depends on the exact nonwoven substrate and film sealant system. The mating substrate should be identified and tested as part of the finished package.
Medical packaging is the application listed in the current HSQY specification. Final suitability must still be confirmed for the specific device, sealing substrate, sterilization process and packaging-system requirements.
Medical textiles are included in the product positioning. Buyers should provide the textile type, package dimensions, sterilization process and required package performance for film selection.
The current product source does not publish a specific OTR value. Request OTR data for the exact thickness and structure together with the applicable temperature and humidity test conditions.
A specific WVTR value is not published in the current source. Buyers requiring defined moisture-barrier performance should provide the target and test conditions.
No EVOH layer is identified in the current PA/PE specification. HSQY has separate EVOH-containing multilayer films for applications requiring enhanced oxygen-barrier performance.
Yes. Printable configurations are listed in the current specification. Confirm printing method, surface treatment, inks and sterilization requirements before production.
The supplied source does not confirm EO qualification for this exact PA/PE grade. Provide the intended sterilization method and cycle so compatibility and supporting documentation can be evaluated.
Compatibility with radiation sterilization is not established by the supplied product details. The exact film grade and finished packaging system should be evaluated under the intended dose and process.
Steam sterilization compatibility is not confirmed in the current PA/PE source. High-temperature sterilization requirements should be provided before material selection because different polymer structures can behave differently under steam conditions.
The supplied product source does not establish product-specific ISO 11607 compliance. For terminally sterilized medical devices, buyers should request applicable material and packaging documentation and validate the complete sterile-barrier packaging system according to relevant requirements.
Not by itself. General company or material certificates should not be interpreted as approval of every film configuration for a particular sterile medical packaging system.
Seal temperature, pressure and dwell time depend on the film grade, mating substrate and packaging machine. The optimum seal window should be established and validated using the actual packaging system.
A specific peel-force value is not published in the current source. Buyers should provide the desired opening requirement and mating substrate so the selected grade can be evaluated.
Core diameter and maximum roll OD are not provided in the current specification. Include packaging-machine roll requirements when requesting a quotation.
The current HSQY product information lists approximately 10-14 working days depending on specification and order quantity. Final production timing should be confirmed when the order is placed.
Provide film thickness, roll width, medical product type, mating substrate, peel requirement, barrier requirement, sterilization method, packaging machine, printing requirement, technical documentation requirement, quantity and destination.
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