GUDIDData
eudamed_udi Primary ID: 06931923800337

dermagel plus orthopedic (UDI 06931923800337)

Manufactured by Guilin HBM Health Protections, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for dermagel plus orthopedic - Primary ID 06931923800337

Device Regulatory Overview

The dermagel plus orthopedic (Model/Catalog Number: RC10063075_2937) is a medical device manufactured by Guilin HBM Health Protections, Inc.. This product is indexed under FDA Product Code / Category Classification T01010102 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
RC10063075_2937
Product Code / EMDN
T01010102
Device Name
Powder free natural rubber latex surgical gloves
Database Sync Date
2026-08-09 17:23:12

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 dermagel plus orthopedic?

The registered manufacturer of record for dermagel plus orthopedic is Guilin HBM Health Protections, Inc..

What is the Primary UDI-DI identifier for dermagel plus orthopedic?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06931923800337.

What classification code is assigned to this device?

This device is registered under product classification code T01010102.

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