eudamed_udi
Primary ID: 04029839993372
Titan-Spongiosaschraube steril (UDI 04029839993372)
Manufactured by Peter Brehm GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Titan-Spongiosaschraube steril - Primary ID 04029839993372
Device Regulatory Overview
The Titan-Spongiosaschraube steril (Model/Catalog Number: 51165115+01) is a medical device manufactured by Peter Brehm GmbH. This product is indexed under FDA Product Code / Category Classification P09088007 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 51165115+01
- Product Code / EMDN
- P09088007
- Device Name
- Titan-Spongiosaschraube steril
- Database Sync Date
- 2026-08-09 16:28:56
Full Regulatory Attributes
đź”’ 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 Titan-Spongiosaschraube steril?
The registered manufacturer of record for Titan-Spongiosaschraube steril is Peter Brehm GmbH.
What is the Primary UDI-DI identifier for Titan-Spongiosaschraube steril?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04029839993372.
What classification code is assigned to this device?
This device is registered under product classification code P09088007.
Similar Classification Devices (P09088007)
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