GUDIDData
eudamed_udi Primary ID: 06933506092344

Sterix Supreme Soft PF Size 6.5 (UDI 06933506092344)

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 Sterix Supreme Soft PF Size 6.5 - Primary ID 06933506092344

Device Regulatory Overview

The Sterix Supreme Soft PF Size 6.5 (Model/Catalog Number: 372GS165) 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
372GS165
Product Code / EMDN
T01010102
Device Name
Powder free natural rubber latex surgical gloves
Database Sync Date
2026-08-09 16:47:22

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 Sterix Supreme Soft PF Size 6.5?

The registered manufacturer of record for Sterix Supreme Soft PF Size 6.5 is Guilin HBM Health Protections, Inc..

What is the Primary UDI-DI identifier for Sterix Supreme Soft PF Size 6.5?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06933506092344.

What classification code is assigned to this device?

This device is registered under product classification code T01010102.

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