eudamed_udi
Primary ID: 04049852302647
BMM Modular Acetabular Inlay (UDI 04049852302647)
Manufactured by Biotech GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BMM Modular Acetabular Inlay - Primary ID 04049852302647
Device Regulatory Overview
The BMM Modular Acetabular Inlay (Model/Catalog Number: 022-2142-3536) is a medical device manufactured by Biotech GmbH. This product is indexed under FDA Product Code / Category Classification P090803050102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 022-2142-3536
- Product Code / EMDN
- P090803050102
- Device Name
- Biotech Acetabular Cup System
- Database Sync Date
- 2026-08-09 16:28:54
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 BMM Modular Acetabular Inlay?
The registered manufacturer of record for BMM Modular Acetabular Inlay is Biotech GmbH.
What is the Primary UDI-DI identifier for BMM Modular Acetabular Inlay?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04049852302647.
What classification code is assigned to this device?
This device is registered under product classification code P090803050102.
Similar Classification Devices (P090803050102)
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