eudamed_udi Primary ID: 03607360047675

MULTI-SYSTEM Hb A1c CAPILLARY CONTROLS (10x2) (UDI 03607360047675)

Manufactured by sebia

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The MULTI-SYSTEM Hb A1c CAPILLARY CONTROLS (10x2) (Model/Catalog Number: 4767) is a medical device manufactured by sebia. This product is indexed under FDA Product Code / Category Classification W0101050205 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 4767
Product Code / EMDN: W0101050205
Device Name: MULTI-SYSTEM Hb A1c CAPILLARY CONTROLS (10x2)
Database Sync Date: 2026-08-09 16:46:38

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 MULTI-SYSTEM Hb A1c CAPILLARY CONTROLS (10x2)?

The registered manufacturer of record for MULTI-SYSTEM Hb A1c CAPILLARY CONTROLS (10x2) is sebia.

What is the Primary UDI-DI identifier for MULTI-SYSTEM Hb A1c CAPILLARY CONTROLS (10x2)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03607360047675.

What classification code is assigned to this device?

This device is registered under product classification code W0101050205.

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