eudamed_udi
Primary ID: 05032384124817
SHEEP BLOOD DEFIBRINATED (UDI 05032384124817)
Manufactured by Oxoid Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SHEEP BLOOD DEFIBRINATED - Primary ID 05032384124817
Device Regulatory Overview
The SHEEP BLOOD DEFIBRINATED (Model/Catalog Number: SR0051C) is a medical device manufactured by Oxoid Ltd. This product is indexed under FDA Product Code / Category Classification W0104010104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SR0051C
- Product Code / EMDN
- W0104010104
- Device Name
- SHEEP BLOOD DEFIBRINATED
- Database Sync Date
- 2026-08-09 17:22:02
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 SHEEP BLOOD DEFIBRINATED?
The registered manufacturer of record for SHEEP BLOOD DEFIBRINATED is Oxoid Ltd.
What is the Primary UDI-DI identifier for SHEEP BLOOD DEFIBRINATED?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05032384124817.
What classification code is assigned to this device?
This device is registered under product classification code W0104010104.
Similar Classification Devices (W0104010104)
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