eudamed_udi
Primary ID: 09551004206857
KBM (UDI 09551004206857)
Manufactured by TG MEDICAL SDN. BHD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KBM - Primary ID 09551004206857
Device Regulatory Overview
The KBM (Model/Catalog Number: 518175) is a medical device manufactured by TG MEDICAL SDN. BHD.. This product is indexed under FDA Product Code / Category Classification T01010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 518175
- Product Code / EMDN
- T01010102
- Device Name
- Sterile Latex Surgical Powder Free Glove
- Database Sync Date
- 2026-08-09 16:49:54
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 KBM?
The registered manufacturer of record for KBM is TG MEDICAL SDN. BHD..
What is the Primary UDI-DI identifier for KBM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09551004206857.
What classification code is assigned to this device?
This device is registered under product classification code T01010102.
Similar Classification Devices (T01010102)
Other Devices by TG MEDICAL SDN. BHD.
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