GUDIDData
eudamed_udi Primary ID: 08681190364664

W 604-M / WOVEN MALLEOL ANKLE SUPPORT (MEDIUM) (UDI 08681190364664)

Manufactured by Doğam Medikal Kozmetik LTD. STI.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for W 604-M / WOVEN MALLEOL ANKLE SUPPORT (MEDIUM) - Primary ID 08681190364664

Device Regulatory Overview

The W 604-M / WOVEN MALLEOL ANKLE SUPPORT (MEDIUM) (Model/Catalog Number: W 604-M) is a medical device manufactured by Doğam Medikal Kozmetik LTD. STI.. This product is indexed under FDA Product Code / Category Classification Y061218 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
W 604-M
Product Code / EMDN
Y061218
Device Name
ANKLE SUPPORTS, WALKERS, WEIGHTS
Database Sync Date
2026-08-09 16:46:00

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 W 604-M / WOVEN MALLEOL ANKLE SUPPORT (MEDIUM)?

The registered manufacturer of record for W 604-M / WOVEN MALLEOL ANKLE SUPPORT (MEDIUM) is Doğam Medikal Kozmetik LTD. STI..

What is the Primary UDI-DI identifier for W 604-M / WOVEN MALLEOL ANKLE SUPPORT (MEDIUM)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08681190364664.

What classification code is assigned to this device?

This device is registered under product classification code Y061218.

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