eudamed_udi
Primary ID: 07090072190009
Fastlegenes KI-verktøy med VideoLege (UDI 07090072190009)
Manufactured by Grini Tech AS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Fastlegenes KI-verktøy med VideoLege - Primary ID 07090072190009
Device Regulatory Overview
The Fastlegenes KI-verktøy med VideoLege (Model/Catalog Number: FKI-5.0) is a medical device manufactured by Grini Tech AS. This product is indexed under FDA Product Code / Category Classification V92 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FKI-5.0
- Product Code / EMDN
- V92
- Device Name
- Fastlegenes KI-verktøy med VideoLege
- Database Sync Date
- 2026-08-09 16:28:52
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 Fastlegenes KI-verktøy med VideoLege?
The registered manufacturer of record for Fastlegenes KI-verktøy med VideoLege is Grini Tech AS.
What is the Primary UDI-DI identifier for Fastlegenes KI-verktøy med VideoLege?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07090072190009.
What classification code is assigned to this device?
This device is registered under product classification code V92.
Similar Classification Devices (V92)
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