MH II agarskål med hemoglobin og isovitalex (UDI 07073097800153)
Manufactured by Oslo universitetssykehus HF
Device Regulatory Overview
The MH II agarskål med hemoglobin og isovitalex (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
- MH II agarskål med hemoglobin og isovitalex
- Database Sync Date
- 2026-08-09 16:29:36
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 MH II agarskål med hemoglobin og isovitalex?
The registered manufacturer of record for MH II agarskål med hemoglobin og isovitalex is Oslo universitetssykehus HF.
What is the Primary UDI-DI identifier for MH II agarskål med hemoglobin og isovitalex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07073097800153.
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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