GUDIDData
eudamed_udi Primary ID: 07332414201609

AK 98 (UDI 07332414201609)

Manufactured by Vantive Health GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AK 98 - Primary ID 07332414201609

Device Regulatory Overview

The AK 98 (Model/Catalog Number: 956014) is a medical device manufactured by Vantive Health GmbH. This product is indexed under FDA Product Code / Category Classification Z12090201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
956014
Product Code / EMDN
Z12090201
Device Name
AK 98
Database Sync Date
2026-08-09 16:29:04

Full Regulatory Attributes

🔒 Token Gated
{
    "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 AK 98?

The registered manufacturer of record for AK 98 is Vantive Health GmbH.

What is the Primary UDI-DI identifier for AK 98?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07332414201609.

What classification code is assigned to this device?

This device is registered under product classification code Z12090201.

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