GUDIDData
eudamed_udi Primary ID: 08680853103404

NEOPRENE WRIST SUPPORT-LEFT-L (UDI 08680853103404)

Manufactured by HEGELİ ORTOPEDİK ÜRÜNLER SAN.LTD.ŞTİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NEOPRENE WRIST SUPPORT-LEFT-L - Primary ID 08680853103404

Device Regulatory Overview

The NEOPRENE WRIST SUPPORT-LEFT-L (Model/Catalog Number: ARH2601-L-LRG) is a medical device manufactured by HEGELİ ORTOPEDİK ÜRÜNLER SAN.LTD.ŞTİ. This product is indexed under FDA Product Code / Category Classification Y060609 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
ARH2601-L-LRG
Product Code / EMDN
Y060609
Device Name
HAND&WRIST
Database Sync Date
2026-08-09 16:29:23

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 NEOPRENE WRIST SUPPORT-LEFT-L?

The registered manufacturer of record for NEOPRENE WRIST SUPPORT-LEFT-L is HEGELİ ORTOPEDİK ÜRÜNLER SAN.LTD.ŞTİ.

What is the Primary UDI-DI identifier for NEOPRENE WRIST SUPPORT-LEFT-L?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08680853103404.

What classification code is assigned to this device?

This device is registered under product classification code Y060609.

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