Stericlin® See-through pouches made of DuPont™ Tyvek® and film (UDI 54009445250033)
Manufactured by Vereinigte Papierwarenfabriken GmbH
Device Regulatory Overview
The Stericlin® See-through pouches made of DuPont™ Tyvek® and film (Model/Catalog Number: 3FKFB250115) is a medical device manufactured by Vereinigte Papierwarenfabriken GmbH. This product is indexed under FDA Product Code / Category Classification S01010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3FKFB250115
- Product Code / EMDN
- S01010201
- Device Name
- Stericlin® See-through packaging made of DuPont™ Tyvek® and film
- Database Sync Date
- 2026-08-09 16:51:06
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Stericlin® See-through pouches made of DuPont™ Tyvek® and film?
The registered manufacturer of record for Stericlin® See-through pouches made of DuPont™ Tyvek® and film is Vereinigte Papierwarenfabriken GmbH.
What is the Primary UDI-DI identifier for Stericlin® See-through pouches made of DuPont™ Tyvek® and film?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 54009445250033.
What classification code is assigned to this device?
This device is registered under product classification code S01010201.
Similar Classification Devices (S01010201)
Other Devices by Vereinigte Papierwarenfabriken GmbH
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