GUDIDData
eudamed_udi Primary ID: 04050598169906

Chymotrypsin-Aktivität (UDI 04050598169906)

Manufactured by Immundiagnostik AG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Chymotrypsin-Aktivität - Primary ID 04050598169906

Device Regulatory Overview

The Chymotrypsin-Aktivität (Model/Catalog Number: K 6990) is a medical device manufactured by Immundiagnostik AG. This product is indexed under FDA Product Code / Category Classification W01010112 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
K 6990
Product Code / EMDN
W01010112
Device Name
Chymotrypsin Activity
Database Sync Date
2026-08-09 16:47:20

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 Chymotrypsin-Aktivität?

The registered manufacturer of record for Chymotrypsin-Aktivität is Immundiagnostik AG.

What is the Primary UDI-DI identifier for Chymotrypsin-Aktivität?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04050598169906.

What classification code is assigned to this device?

This device is registered under product classification code W01010112.

Similar Classification Devices (W01010112)

Other Devices by Immundiagnostik AG

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