GUDIDData
eudamed_udi Primary ID: 07090064750020

GA-map® Sample Collection Kit (UDI 07090064750020)

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® Sample Collection Kit - Primary ID 07090064750020

Device Regulatory Overview

The GA-map® Sample Collection Kit (Model/Catalog Number: 1020) is a medical device manufactured by Genetic Analysis AS. This product is indexed under FDA Product Code / Category Classification A1102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1020
Product Code / EMDN
A1102
Device Name
GA-map® Sample Collection Kit
Database Sync Date
2026-08-09 16:29:24

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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Frequently Asked Questions

Who is the primary manufacturer of GA-map® Sample Collection Kit?

The registered manufacturer of record for GA-map® Sample Collection Kit is Genetic Analysis AS.

What is the Primary UDI-DI identifier for GA-map® Sample Collection Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07090064750020.

What classification code is assigned to this device?

This device is registered under product classification code A1102.

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