GUDIDData
eudamed_udi Primary ID: 08685126711713

GPAD PECTUS CARINATUM POSTURE CORRECTION BRACE 43234 LL (UDI 08685126711713)

Manufactured by TEDOB PRODÜKSİYON SAĞLIK VE GIDA SAN. VE TİC. LTD. ŞTİ.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GPAD PECTUS CARINATUM POSTURE CORRECTION BRACE 43234 LL - Primary ID 08685126711713

Device Regulatory Overview

The GPAD PECTUS CARINATUM POSTURE CORRECTION BRACE 43234 LL (Model/Catalog Number: GP43234LL) is a medical device manufactured by TEDOB PRODÜKSİYON SAĞLIK VE GIDA SAN. VE TİC. LTD. ŞTİ.. This product is indexed under FDA Product Code / Category Classification Y061219 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
GP43234LL
Product Code / EMDN
Y061219
Device Name
GPAD PUCTUS CARINATUM POSTURE CORRECTION BRACE
Database Sync Date
2026-08-09 16:46:54

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 GPAD PECTUS CARINATUM POSTURE CORRECTION BRACE 43234 LL?

The registered manufacturer of record for GPAD PECTUS CARINATUM POSTURE CORRECTION BRACE 43234 LL is TEDOB PRODÜKSİYON SAĞLIK VE GIDA SAN. VE TİC. LTD. ŞTİ..

What is the Primary UDI-DI identifier for GPAD PECTUS CARINATUM POSTURE CORRECTION BRACE 43234 LL?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08685126711713.

What classification code is assigned to this device?

This device is registered under product classification code Y061219.

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