eudamed_udi
Primary ID: 04049852292948
Biotech Modular Revision Hip Stem - Screw (UDI 04049852292948)
Manufactured by Biotech GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Biotech Modular Revision Hip Stem - Screw - Primary ID 04049852292948
Device Regulatory Overview
The Biotech Modular Revision Hip Stem - Screw (Model/Catalog Number: 008-1111-0010) is a medical device manufactured by Biotech GmbH. This product is indexed under FDA Product Code / Category Classification P09088007 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 008-1111-0010
- Product Code / EMDN
- P09088007
- Device Name
- Biotech Modular Revision Hip Stem System
- Database Sync Date
- 2026-08-09 16:49:51
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 Biotech Modular Revision Hip Stem - Screw?
The registered manufacturer of record for Biotech Modular Revision Hip Stem - Screw is Biotech GmbH.
What is the Primary UDI-DI identifier for Biotech Modular Revision Hip Stem - Screw?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04049852292948.
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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