dermagel plus dual (UDI 06931923800375)
Manufactured by Guilin HBM Health Protections, Inc.
Device Regulatory Overview
The dermagel plus dual (Model/Catalog Number: RC10064055_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
- RC10064055_2937
- Product Code / EMDN
- T01010102
- Device Name
- Powder free natural rubber latex surgical gloves
- Database Sync Date
- 2026-08-09 16:50:10
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 dermagel plus dual?
The registered manufacturer of record for dermagel plus dual is Guilin HBM Health Protections, Inc..
What is the Primary UDI-DI identifier for dermagel plus dual?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06931923800375.
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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