eudamed_udi
Primary ID: 09555076113457
Ulma Fortis (UDI 09555076113457)
Manufactured by TERANG NUSA (MALAYSIA) SDN. BHD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ulma Fortis - Primary ID 09555076113457
Device Regulatory Overview
The Ulma Fortis (Model/Catalog Number: UMF-507611345) is a medical device manufactured by TERANG NUSA (MALAYSIA) 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
- UMF-507611345
- Product Code / EMDN
- T01010102
- Device Name
- Sterile Latex Surgical Powder Free Glove
- Database Sync Date
- 2026-08-09 16:29:52
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 Ulma Fortis?
The registered manufacturer of record for Ulma Fortis is TERANG NUSA (MALAYSIA) SDN. BHD..
What is the Primary UDI-DI identifier for Ulma Fortis?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09555076113457.
What classification code is assigned to this device?
This device is registered under product classification code T01010102.
Similar Classification Devices (T01010102)
Other Devices by TERANG NUSA (MALAYSIA) SDN. BHD.
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