Sterix supremesoft PP, size 6.0 (UDI 06931923805943)
Manufactured by Guilin HBM Health Protections, Inc.
Device Regulatory Overview
The Sterix supremesoft PP, size 6.0 (Model/Catalog Number: 371GS160) is a medical device manufactured by Guilin HBM Health Protections, Inc.. This product is indexed under FDA Product Code / Category Classification T01010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 371GS160
- Product Code / EMDN
- T01010101
- Device Name
- Powdered Natural Rubber Latex Surgical Gloves
- Database Sync Date
- 2026-08-09 17:20:40
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Sterix supremesoft PP, size 6.0?
The registered manufacturer of record for Sterix supremesoft PP, size 6.0 is Guilin HBM Health Protections, Inc..
What is the Primary UDI-DI identifier for Sterix supremesoft PP, size 6.0?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06931923805943.
What classification code is assigned to this device?
This device is registered under product classification code T01010101.
Similar Classification Devices (T01010101)
Other Devices by Guilin HBM Health Protections, Inc.
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