GUDIDData
eudamed_udi Primary ID: 08697888887360

POST OPERATİF SÜTYEN(FERMUARLI (SİYAH) (L) (UDI 08697888887360)

Manufactured by ABC TIP SAĞLIK SPOR MALZ. TEKS. TURZ. İNŞ. SAN. VE TİC. LTD. ŞTİ.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for POST OPERATİF SÜTYEN(FERMUARLI (SİYAH) (L) - Primary ID 08697888887360

Device Regulatory Overview

The POST OPERATİF SÜTYEN(FERMUARLI (SİYAH) (L) (Model/Catalog Number: LC 201S(L)) is a medical device manufactured by ABC TIP SAĞLIK SPOR MALZ. TEKS. TURZ. İNŞ. SAN. VE TİC. LTD. ŞTİ.. This product is indexed under FDA Product Code / Category Classification M030499 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
LC 201S(L)
Product Code / EMDN
M030499
Device Name
Çene Kulak Boyun Bandı
Database Sync Date
2026-08-09 16:28:53

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 POST OPERATİF SÜTYEN(FERMUARLI (SİYAH) (L)?

The registered manufacturer of record for POST OPERATİF SÜTYEN(FERMUARLI (SİYAH) (L) is ABC TIP SAĞLIK SPOR MALZ. TEKS. TURZ. İNŞ. SAN. VE TİC. LTD. ŞTİ..

What is the Primary UDI-DI identifier for POST OPERATİF SÜTYEN(FERMUARLI (SİYAH) (L)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08697888887360.

What classification code is assigned to this device?

This device is registered under product classification code M030499.

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