eudamed_udi
Primary ID: 07073097800108
Brucella agarskål (UDI 07073097800108)
Manufactured by Oslo universitetssykehus HF
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Brucella agarskål - Primary ID 07073097800108
Device Regulatory Overview
The Brucella agarskål (Model/Catalog Number: Not applicable) is a medical device manufactured by Oslo universitetssykehus HF. This product is indexed under FDA Product Code / Category Classification W0104010403 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Not applicable
- Product Code / EMDN
- W0104010403
- Device Name
- Brucella agarskål
- Database Sync Date
- 2026-08-09 17:53:04
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 Brucella agarskål?
The registered manufacturer of record for Brucella agarskål is Oslo universitetssykehus HF.
What is the Primary UDI-DI identifier for Brucella agarskål?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07073097800108.
What classification code is assigned to this device?
This device is registered under product classification code W0104010403.
Similar Classification Devices (W0104010403)
Other Devices by Oslo universitetssykehus HF
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