Modular Acetabular Metal Inlay for Unipolar head (UDI 04049852207928)
Manufactured by Biotech GmbH
Device Regulatory Overview
The Modular Acetabular Metal Inlay for Unipolar head (Model/Catalog Number: 022-2136-5242) is a medical device manufactured by Biotech GmbH. This product is indexed under FDA Product Code / Category Classification P090803010299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 022-2136-5242
- Product Code / EMDN
- P090803010299
- Device Name
- Biotech Acetabular Cup System
- Database Sync Date
- 2026-08-09 16:28:56
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 Modular Acetabular Metal Inlay for Unipolar head?
The registered manufacturer of record for Modular Acetabular Metal Inlay for Unipolar head is Biotech GmbH.
What is the Primary UDI-DI identifier for Modular Acetabular Metal Inlay for Unipolar head?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04049852207928.
What classification code is assigned to this device?
This device is registered under product classification code P090803010299.
Similar Classification Devices (P090803010299)
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