eudamed_udi Primary ID: 08698918067424

Kompres (Batın) 40 cm x 40 cm (4-6-8-12-16 katlı) (UDI 08698918067424)

Manufactured by A.C.S. TIBBİ TEKSTİL ÜRÜNLERİ SAN.VE TİC. LTD.ŞTİ

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Kompres (Batın) 40 cm x 40 cm (4-6-8-12-16 katlı) (Model/Catalog Number: A-208) is a medical device manufactured by A.C.S. TIBBİ TEKSTİL ÜRÜNLERİ SAN.VE TİC. LTD.ŞTİ. This product is indexed under FDA Product Code / Category Classification M0201020102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: A-208
Product Code / EMDN: M0201020102
Device Name: Kompres (Batın)
Database Sync Date: 2026-08-09 16:29:41

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 Kompres (Batın) 40 cm x 40 cm (4-6-8-12-16 katlı)?

The registered manufacturer of record for Kompres (Batın) 40 cm x 40 cm (4-6-8-12-16 katlı) is A.C.S. TIBBİ TEKSTİL ÜRÜNLERİ SAN.VE TİC. LTD.ŞTİ.

What is the Primary UDI-DI identifier for Kompres (Batın) 40 cm x 40 cm (4-6-8-12-16 katlı)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08698918067424.

What classification code is assigned to this device?

This device is registered under product classification code M0201020102.

Similar Classification Devices (M0201020102)

Other Devices by A.C.S. TIBBİ TEKSTİL ÜRÜNLERİ SAN.VE TİC. LTD.ŞTİ

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