GUDIDData
eudamed_udi Primary ID: 08682495015299

BD 716 7 / (UDI 08682495015299)

Manufactured by BİOAKTİF TIBBİ ÜRÜNLER VE TEKNİK TEKSTİL SAN. TİC. LTD. ŞTİ.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BD 716 7 / - Primary ID 08682495015299

Device Regulatory Overview

The BD 716 7 / (Model/Catalog Number: BD 716 7) is a medical device manufactured by BİOAKTİF TIBBİ ÜRÜNLER VE TEKNİK TEKSTİL SAN. TİC. LTD. ŞTİ.. This product is indexed under FDA Product Code / Category Classification M030405 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
BD 716 7
Product Code / EMDN
M030405
Device Name
VARICOSE AND ANTI-EMBOLISM STOCKINGS
Database Sync Date
2026-08-09 16:28:57

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 BD 716 7 /?

The registered manufacturer of record for BD 716 7 / is BİOAKTİF TIBBİ ÜRÜNLER VE TEKNİK TEKSTİL SAN. TİC. LTD. ŞTİ..

What is the Primary UDI-DI identifier for BD 716 7 /?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682495015299.

What classification code is assigned to this device?

This device is registered under product classification code M030405.

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