eudamed_udi
Primary ID: 04051308047170
Führungshülse Repomadenschraubendreher (UDI 04051308047170)
Manufactured by Peter Brehm GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Führungshülse Repomadenschraubendreher - Primary ID 04051308047170
Device Regulatory Overview
The Führungshülse Repomadenschraubendreher (Model/Catalog Number: 22600-150) is a medical device manufactured by Peter Brehm GmbH. This product is indexed under FDA Product Code / Category Classification L091199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 22600-150
- Product Code / EMDN
- L091199
- Device Name
- Führungshülse Repomadenschraubendreher
- Database Sync Date
- 2026-08-09 16:28:49
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 Führungshülse Repomadenschraubendreher?
The registered manufacturer of record for Führungshülse Repomadenschraubendreher is Peter Brehm GmbH.
What is the Primary UDI-DI identifier for Führungshülse Repomadenschraubendreher?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04051308047170.
What classification code is assigned to this device?
This device is registered under product classification code L091199.
Similar Classification Devices (L091199)
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