VERANKERUNGSSCHAFT gebogen zementfrei (UDI 04029839311176)
Manufactured by Peter Brehm GmbH
Device Regulatory Overview
The VERANKERUNGSSCHAFT gebogen zementfrei (Model/Catalog Number: 42731-03) is a medical device manufactured by Peter Brehm GmbH. This product is indexed under FDA Product Code / Category Classification P0909800601,P0909800602 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 42731-03
- Product Code / EMDN
- P0909800601,P0909800602
- Device Name
- VERANKERUNGSSCHAFT gebogen zementfrei
- Database Sync Date
- 2026-08-09 17:07:33
Full Regulatory Attributes
đź”’ Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of VERANKERUNGSSCHAFT gebogen zementfrei?
The registered manufacturer of record for VERANKERUNGSSCHAFT gebogen zementfrei is Peter Brehm GmbH.
What is the Primary UDI-DI identifier for VERANKERUNGSSCHAFT gebogen zementfrei?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04029839311176.
What classification code is assigned to this device?
This device is registered under product classification code P0909800601,P0909800602.
Similar Classification Devices (P0909800601,P0909800602)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint