GUDIDData
eudamed_udi Primary ID: 06931923800146

dermagel plus coated (UDI 06931923800146)

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 coated - Primary ID 06931923800146

Device Regulatory Overview

The dermagel plus coated (Model/Catalog Number: RC10061060_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
RC10061060_2937
Product Code / EMDN
T01010102
Device Name
Powder free natural rubber latex surgical gloves
Database Sync Date
2026-08-09 17:27:14

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 coated?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06931923800146.

What classification code is assigned to this device?

This device is registered under product classification code T01010102.

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