GUDIDData
eudamed_udi Primary ID: 08697409379886

15 cm x 2 m. Hidrofil Sargı Bezi (UDI 08697409379886)

Manufactured by TEMAŞ TIBBİ MALZEMELER VE SARGI BEZİ SANAYİ VE TİCARET ANONİM ŞİRKETİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for 15 cm x 2 m. Hidrofil Sargı Bezi - Primary ID 08697409379886

Device Regulatory Overview

The 15 cm x 2 m. Hidrofil Sargı Bezi (Model/Catalog Number: KT1003) is a medical device manufactured by TEMAŞ TIBBİ MALZEMELER VE SARGI BEZİ SANAYİ VE TİCARET ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification M0299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
KT1003
Product Code / EMDN
M0299
Device Name
Bandaj ve Sargı Bezleri
Database Sync Date
2026-08-09 16:48:37

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 15 cm x 2 m. Hidrofil Sargı Bezi?

The registered manufacturer of record for 15 cm x 2 m. Hidrofil Sargı Bezi is TEMAŞ TIBBİ MALZEMELER VE SARGI BEZİ SANAYİ VE TİCARET ANONİM ŞİRKETİ.

What is the Primary UDI-DI identifier for 15 cm x 2 m. Hidrofil Sargı Bezi?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08697409379886.

What classification code is assigned to this device?

This device is registered under product classification code M0299.

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