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Nylon Thermoforming Film — Medical Care Package
F2615-M is a 120μm NY/PE deep-draw vacuum thermoforming base film for sterilized medical equipment, supporting forming depths up to 30mm for bulkier devices, and suitable for E.O. or gamma (r-ray) sterilization.
A Deep-Draw Base Film for Sterilized Medical Equipment
F2615-M is the 120μm grade in Intlpak's NE medical series, supporting forming cavities up to 30mm for bulkier devices that the shallower F2624-M grade cannot accommodate. It is produced by computer-controlled co-extrusion with automatic foreign-object detection and thickness control in clean-room conditions, and retains the series' formability, pinhole resistance, and inspection clarity at the heavier gauge.
Where F2615-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 Bulkier sterilized medical equipment requiring a deeper forming cavity
- 4 Packaging lines requiring E.O. or gamma (r-ray) sterilization compatibility
Full Specifications — Nylon/PE Medical Thermoforming Film Series
F2615-M is the 120μm deep-draw grade in Intlpak's NE nylon/PE medical thermoforming film family. The table below shows F2615-M alongside the 80–150μm 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 F2615-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 F2615-M
F2615-M and the food-grade F2615 are the same gauge — are they interchangeable?
No. Both are 120 μm, but F2615 is a food vacuum packaging film while F2615-M is the medical device forming base film specified for E.O. and gamma sterilization. Medical packaging carries sterilization validation and regulatory documentation, so always order by the full part number including the -M suffix.
What devices does F2615-M's 10–30 mm range cover?
Most routine devices — syringes, catheters, suture materials, small instrument sets. Flatter items use less material on F2624-M (10–15 mm), while deep instrument trays need F2606-M (30–50 mm). F2703 at 110 μm is worth comparing at the same depth range.
What is the practical benefit of supporting both E.O. and gamma?
Fewer part numbers and less validation overhead. One film covering both routes means that switching sterilization method, or serving markets that use different processes, requires no change of packaging material — only supplementary qualification for the new process. For device makers selling across multiple markets that is a real simplification of inventory and documentation.
How are top web and sealing settled for F2615-M?
The top web is a breathable medical-grade material — dialysis paper or Tyvek — permitting sterilant exchange. Seal parameters (temperature, pressure, dwell) depend on your actual top web and machine, and must be verified by peel strength and seal integrity testing, then documented within your ISO 11607-related sterile barrier system validation.
How do I obtain quality and cleanliness documentation for F2615-M?
The film is produced in a GMP clean-room under ISO 9001 with raw-material traceability. If your submission requires cleanliness class statements, particulate data or bioburden reports, tell our engineering team your target market and regulatory pathway and we will supply the corresponding documents and samples.