GUDIDData
eudamed_udi Primary ID: 08684072200135

Gauze Compress (Sponge) 5cm x 5cm 12 folds 20 wires Without X-Ray Non-sterile (UDI 08684072200135)

Manufactured by ERMED TIP MEDİKAL TİCARET A.Ş.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Gauze Compress (Sponge) 5cm x 5cm 12 folds 20 wires Without X-Ray Non-sterile - Primary ID 08684072200135

Device Regulatory Overview

The Gauze Compress (Sponge) 5cm x 5cm 12 folds 20 wires Without X-Ray Non-sterile (Model/Catalog Number: ESY50013) is a medical device manufactured by ERMED TIP MEDİKAL TİCARET A.Ş.. This product is indexed under FDA Product Code / Category Classification M0201020102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ESY50013
Product Code / EMDN
M0201020102
Device Name
Sponge and Abdominal Compress Without X-ray Non-Sterile
Database Sync Date
2026-08-09 16:29:59

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 Gauze Compress (Sponge) 5cm x 5cm 12 folds 20 wires Without X-Ray Non-sterile?

The registered manufacturer of record for Gauze Compress (Sponge) 5cm x 5cm 12 folds 20 wires Without X-Ray Non-sterile is ERMED TIP MEDİKAL TİCARET A.Ş..

What is the Primary UDI-DI identifier for Gauze Compress (Sponge) 5cm x 5cm 12 folds 20 wires Without X-Ray Non-sterile?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08684072200135.

What classification code is assigned to this device?

This device is registered under product classification code M0201020102.

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