eudamed_udi
Primary ID: 04051308030226
Handgewindebohrer Mittelschneider (UDI 04051308030226)
Manufactured by Peter Brehm GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Handgewindebohrer Mittelschneider - Primary ID 04051308030226
Device Regulatory Overview
The Handgewindebohrer Mittelschneider (Model/Catalog Number: 12710-04-02) is a medical device manufactured by Peter Brehm GmbH. This product is indexed under FDA Product Code / Category Classification L091102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 12710-04-02
- Product Code / EMDN
- L091102
- Device Name
- Handgewindebohrer Mittelschneider
- Database Sync Date
- 2026-08-09 16:30:03
Full Regulatory Attributes
đ Token Gated
{
"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 Handgewindebohrer Mittelschneider?
The registered manufacturer of record for Handgewindebohrer Mittelschneider is Peter Brehm GmbH.
What is the Primary UDI-DI identifier for Handgewindebohrer Mittelschneider?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04051308030226.
What classification code is assigned to this device?
This device is registered under product classification code L091102.
Similar Classification Devices (L091102)
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