eudamed_udi
Primary ID: 04032651216079
octenisept wound gel (UDI 04032651216079)
Manufactured by Schülke & Mayr GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for octenisept wound gel - Primary ID 04032651216079
Device Regulatory Overview
The octenisept wound gel (Model/Catalog Number: 121607) is a medical device manufactured by Schülke & Mayr GmbH. This product is indexed under FDA Product Code / Category Classification Z12019003 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 121607
- Product Code / EMDN
- Z12019003
- Device Name
- octenisept gel
- Database Sync Date
- 2026-08-09 16:28:55
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 octenisept wound gel?
The registered manufacturer of record for octenisept wound gel is Schülke & Mayr GmbH.
What is the Primary UDI-DI identifier for octenisept wound gel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04032651216079.
What classification code is assigned to this device?
This device is registered under product classification code Z12019003.
Similar Classification Devices (Z12019003)
Other Devices by Schülke & Mayr GmbH
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