eudamed_udi
Primary ID: 06221166001067
Unspecified Brand (UDI 06221166001067)
Manufactured by Allmed Middle East
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 06221166001067
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: BIOPURE 130 LF) is a medical device manufactured by Allmed Middle East. This product is indexed under FDA Product Code / Category Classification F01060103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BIOPURE 130 LF
- Product Code / EMDN
- F01060103
- Device Name
- Biopure Hollow Fiber Haemodialyzers
- Database Sync Date
- 2026-08-09 17:03:17
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Allmed Middle East.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06221166001067.
What classification code is assigned to this device?
This device is registered under product classification code F01060103.
Similar Classification Devices (F01060103)
Other Devices by Allmed Middle East
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