GUDIDData
eudamed_udi Primary ID: 08682132205076

K 522-M / T.L.S.O CORSET SIZE M (UDI 08682132205076)

Manufactured by EFAMED ORTOPEDİ MEDİKAL ÜRÜNLER TİC SAN LTD ŞTİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for K 522-M / T.L.S.O CORSET SIZE M - Primary ID 08682132205076

Device Regulatory Overview

The K 522-M / T.L.S.O CORSET SIZE M (Model/Catalog Number: K 522-M) is a medical device manufactured by EFAMED ORTOPEDİ MEDİKAL ÜRÜNLER TİC SAN LTD ŞTİ. This product is indexed under FDA Product Code / Category Classification Y060380 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
K 522-M
Product Code / EMDN
Y060380
Device Name
CORSET SUPPORTS
Database Sync Date
2026-08-09 16:49:37

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 K 522-M / T.L.S.O CORSET SIZE M?

The registered manufacturer of record for K 522-M / T.L.S.O CORSET SIZE M is EFAMED ORTOPEDİ MEDİKAL ÜRÜNLER TİC SAN LTD ŞTİ.

What is the Primary UDI-DI identifier for K 522-M / T.L.S.O CORSET SIZE M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682132205076.

What classification code is assigned to this device?

This device is registered under product classification code Y060380.

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