GUDIDData
eudamed_udi Primary ID: 08684072220379

Abdominal Compress 30cm x 30cm 8 folds 18 wires Without X-Ray ETO sterile (UDI 08684072220379)

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 Abdominal Compress 30cm x 30cm 8 folds 18 wires Without X-Ray ETO sterile - Primary ID 08684072220379

Device Regulatory Overview

The Abdominal Compress 30cm x 30cm 8 folds 18 wires Without X-Ray ETO sterile (Model/Catalog Number: ESY80365) is a medical device manufactured by ERMED TIP MEDİKAL TİCARET A.Ş.. This product is indexed under FDA Product Code / Category Classification M0201020101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ESY80365
Product Code / EMDN
M0201020101
Device Name
Sponge and Abdominal Compress Without X-ray Sterile
Database Sync Date
2026-08-09 16:29:10

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 Abdominal Compress 30cm x 30cm 8 folds 18 wires Without X-Ray ETO sterile?

The registered manufacturer of record for Abdominal Compress 30cm x 30cm 8 folds 18 wires Without X-Ray ETO sterile is ERMED TIP MEDİKAL TİCARET A.Ş..

What is the Primary UDI-DI identifier for Abdominal Compress 30cm x 30cm 8 folds 18 wires Without X-Ray ETO sterile?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08684072220379.

What classification code is assigned to this device?

This device is registered under product classification code M0201020101.

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