GUDIDData
eudamed_udi Primary ID: 04030155019493

Cuff A3, black, 2 tubes child (UDI 04030155019493)

Manufactured by Kirchner & Wilhelm GmbH + Co KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cuff A3, black, 2 tubes child - Primary ID 04030155019493

Device Regulatory Overview

The Cuff A3, black, 2 tubes child (Model/Catalog Number: 04.86600.221) is a medical device manufactured by Kirchner & Wilhelm GmbH + Co KG. This product is indexed under FDA Product Code / Category Classification C9006 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
04.86600.221
Product Code / EMDN
C9006
Device Name
Aneroid sphygmomanometers
Database Sync Date
2026-08-09 16:45:53

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 Cuff A3, black, 2 tubes child?

The registered manufacturer of record for Cuff A3, black, 2 tubes child is Kirchner & Wilhelm GmbH + Co KG.

What is the Primary UDI-DI identifier for Cuff A3, black, 2 tubes child?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04030155019493.

What classification code is assigned to this device?

This device is registered under product classification code C9006.

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