eudamed_udi
Primary ID: 04262432771217
Zensiv (UDI 04262432771217)
Manufactured by Oxmed International GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Zensiv - Primary ID 04262432771217
Device Regulatory Overview
The Zensiv (Model/Catalog Number: D1FB10) is a medical device manufactured by Oxmed International GmbH. This product is indexed under FDA Product Code / Category Classification A1001020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- D1FB10
- Product Code / EMDN
- A1001020102
- Device Name
- Zensiv 1-piece Ileostomy pouches
- Database Sync Date
- 2026-08-09 16:59:12
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 Zensiv?
The registered manufacturer of record for Zensiv is Oxmed International GmbH.
What is the Primary UDI-DI identifier for Zensiv?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04262432771217.
What classification code is assigned to this device?
This device is registered under product classification code A1001020102.
Similar Classification Devices (A1001020102)
Other Devices by Oxmed International GmbH
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