eudamed_udi
Primary ID: D-01001DP
GA-map® Dysbiosis Test Lx v2 (UDI D-01001DP)
Manufactured by Genetic Analysis AS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GA-map® Dysbiosis Test Lx v2 - Primary ID D-01001DP
Device Regulatory Overview
The GA-map® Dysbiosis Test Lx v2 (Model/Catalog Number: 1001) is a medical device manufactured by Genetic Analysis AS. This product is indexed under FDA Product Code / Category Classification W010699 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1001
- Product Code / EMDN
- W010699
- Device Name
- GA-map® Dysbiosis Test Lx v2
- Database Sync Date
- 2026-08-09 17:29:10
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 GA-map® Dysbiosis Test Lx v2?
The registered manufacturer of record for GA-map® Dysbiosis Test Lx v2 is Genetic Analysis AS.
What is the Primary UDI-DI identifier for GA-map® Dysbiosis Test Lx v2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-01001DP.
What classification code is assigned to this device?
This device is registered under product classification code W010699.
Similar Classification Devices (W010699)
Other Devices by Genetic Analysis AS
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