GUDIDData
eudamed_udi Primary ID: 06931923801310

dermagel plus PI micro (UDI 06931923801310)

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 PI micro - Primary ID 06931923801310

Device Regulatory Overview

The dermagel plus PI micro (Model/Catalog Number: RC50067080_2937) is a medical device manufactured by Guilin HBM Health Protections, Inc.. This product is indexed under FDA Product Code / Category Classification T01010203 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
RC50067080_2937
Product Code / EMDN
T01010203
Device Name
Powder free synthetic polyisoprene surgical gloves
Database Sync Date
2026-08-09 17:08:13

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 PI micro?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06931923801310.

What classification code is assigned to this device?

This device is registered under product classification code T01010203.

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