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Nylon Thermoforming Film — Medical Care Package
F2624-M is an 80μm NY/PE vacuum thermoforming base film purpose-built for medical device packaging — injection syringes, gauze, cotton pads, suction tubes, and other disposable medical supplies — suitable for either E.O. (ethylene oxide) or gamma (r-ray) sterilization.
A Nylon/PE Base Film Built for Sterile Medical Packaging
F2624-M is the 80μm entry gauge of Intlpak's NE medical series, running as the forming (base) film at a 10–15mm draw. It is produced by computer-controlled co-extrusion with automatic foreign-object detection and thickness control under clean-room standards, and pairs the best formability and pinhole resistance in its gauge class with the transparency and gloss needed for clear device inspection.
Where F2624-M Is Used
- 1 Vacuum thermoforming base film for disposable medical supplies and medical equipment
- 2 Injection syringes, gauze, cotton pads, and sputum suction tubes
- 3 Other single-use medical devices requiring shallow vacuum-formed packaging
- 4 Packaging lines requiring E.O. or gamma (r-ray) sterilization compatibility
Full Specifications — Nylon/PE Medical Thermoforming Film Series
F2624-M is the 80μm shallow-draw grade in Intlpak's NE nylon/PE medical thermoforming film family. The table below shows F2624-M alongside the deeper-draw 110–150μm grades in the same series.
| Property | F2624-M (80μm) | F2703 (110μm) | F2615-M (120μm) | F2606-M (150μm) |
|---|---|---|---|---|
| Thickness | 80 μm | 110 μm | 120 μm | 150 μm |
| Suggested Forming Depth | 10–15 mm | 10–30 mm | 10–30 mm | 30–50 mm |
| Formability / Pinhole Resistance | Best-in-class across the series | |||
| Optical Properties | High transparency, high gloss | |||
| Sterilization Compatibility | E.O. and gamma (r-ray) | E.O. and gamma (r-ray) | E.O. and gamma (r-ray) | E.O. and gamma (r-ray) |
| Typical Application | Injection syringes, gauze, cotton pads, suction tubes, and other medical equipment | |||
| Width | Customized | |||
| Length | Customized | |||
Reviewed by: Intlpak R&D Team.
Why F2624-M Performs
Storage Notice
Avoid exposure to direct light, wind, and rain — store under appropriate conditions. Prevent products from slipping from high places, being polluted, or being impacted during handling.
Quality & Certification
Manufactured under ISO 9001 quality management and GMP clean-room production standards suited to medical-grade packaging, with ISO 22000 & HACCP certification. All products undergo annual safety checks.
Questions About F2624-M
F2624-M takes both E.O. and gamma — how does it compare with the E.O.-only F4538?
It depends on whether your sterilization route might change. F4538 (MPP/PE, 80 μm) is E.O. only; F2624-M matches it at 80 μm and the same 10–15 mm shallow draw while accepting E.O. and gamma. If your line may switch methods, or different markets use different processes, F2624-M keeps that option open.
Does gamma irradiation yellow or embrittle nylon?
Managing that is exactly what a medical-grade nylon formulation is for. F2624-M is specified as gamma (r-ray) compatible, meaning the formulation holds mechanical properties and acceptable appearance at standard doses. Dose, dose rate and storage conditions all affect outcomes, so qualify post-sterilization performance and ageing at your actual dose before adoption.
What is F2624-M's forming limit, and what if I exceed it?
15 mm. Beyond that, step up: F2615-M (120 μm) covers 10–30 mm, F2606-M (150 μm) covers 30–50 mm, and F2703 (110 μm) also spans 10–30 mm. All four are dual E.O./gamma compatible, so changing depth doesn't change your sterilization validation logic.
What top web pairs with F2624-M?
A breathable one — medical-grade dialysis paper or Tyvek — allowing sterilant exchange while maintaining the microbial barrier. F2624-M is the bottom web, thermoformed into the device cavity, and seal parameters should be qualified together with your sterile barrier system under ISO 11607-related requirements.
Does F2624-M's manufacturing environment meet medical packaging expectations?
It is produced in a GMP clean-room under an ISO 9001 quality management system with raw-material traceability. Medical packaging often requires additional cleanliness class, particulate or bioburden documentation for regulatory submission — tell our engineering team your regulatory pathway and we will provide what your filing needs.