GUDIDData
eudamed_udi Primary ID: 06971787073577

SURGITOUCH  H POWDER-FREE SURGICAL GLOVES (UDI 06971787073577)

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 SURGITOUCH  H POWDER-FREE SURGICAL GLOVES - Primary ID 06971787073577

Device Regulatory Overview

The SURGITOUCH  H POWDER-FREE SURGICAL GLOVES (Model/Catalog Number: MA-145-7002-008) 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
MA-145-7002-008
Product Code / EMDN
T01010102
Device Name
Powder free natural rubber latex surgical gloves
Database Sync Date
2026-08-09 17:10:21

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 SURGITOUCH  H POWDER-FREE SURGICAL GLOVES?

The registered manufacturer of record for SURGITOUCH  H POWDER-FREE SURGICAL GLOVES is Guilin HBM Health Protections, Inc..

What is the Primary UDI-DI identifier for SURGITOUCH  H POWDER-FREE SURGICAL GLOVES?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06971787073577.

What classification code is assigned to this device?

This device is registered under product classification code T01010102.

Similar Classification Devices (T01010102)

Other Devices by Guilin HBM Health Protections, Inc.

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