GUDIDData
eudamed_udi Primary ID: 18430155001840

KIT CONTROLES HbA1 (UDI 18430155001840)

Manufactured by QUIMICA CLINICA APLICADA S.A.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KIT CONTROLES HbA1 - Primary ID 18430155001840

Device Regulatory Overview

The KIT CONTROLES HbA1 (Model/Catalog Number: 996636) is a medical device manufactured by QUIMICA CLINICA APLICADA S.A.. This product is indexed under FDA Product Code / Category Classification W0101050205 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
996636
Product Code / EMDN
W0101050205
Device Name
GLUCOHEMOGLOBINA (HbA1), JUEGO DE CONTROLES
Database Sync Date
2026-08-09 17:17:20

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 KIT CONTROLES HbA1?

The registered manufacturer of record for KIT CONTROLES HbA1 is QUIMICA CLINICA APLICADA S.A..

What is the Primary UDI-DI identifier for KIT CONTROLES HbA1?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 18430155001840.

What classification code is assigned to this device?

This device is registered under product classification code W0101050205.

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