eudamed_udi
Primary ID: 04251992197018
Rippenbandage Herren (UDI 04251992197018)
Manufactured by John GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rippenbandage Herren - Primary ID 04251992197018
Device Regulatory Overview
The Rippenbandage Herren (Model/Catalog Number: BANDAGE-04050-H-M-1) is a medical device manufactured by John GmbH. This product is indexed under FDA Product Code / Category Classification M03040199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BANDAGE-04050-H-M-1
- Product Code / EMDN
- M03040199
- Device Name
- Rippenbandage
- Database Sync Date
- 2026-08-09 16:59:47
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 Rippenbandage Herren?
The registered manufacturer of record for Rippenbandage Herren is John GmbH.
What is the Primary UDI-DI identifier for Rippenbandage Herren?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251992197018.
What classification code is assigned to this device?
This device is registered under product classification code M03040199.
Similar Classification Devices (M03040199)
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