gudid
Primary ID: TI-10
PREMIOtitan (UDI TI-10)
Manufactured by PRIMOTEC LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PREMIOtitan - Primary ID TI-10
Device Regulatory Overview
The PREMIOtitan (Model/Catalog Number: TI-10) is a medical device manufactured by PRIMOTEC LLC. This product is indexed under FDA Product Code / Category Classification EJH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TI-10
- Product Code / EMDN
- EJH
- Device Name
- Database Sync Date
- 2026-08-09 09:03:38
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 PREMIOtitan?
The registered manufacturer of record for PREMIOtitan is PRIMOTEC LLC.
What is the Primary UDI-DI identifier for PREMIOtitan?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TI-10.
What classification code is assigned to this device?
This device is registered under product classification code EJH.
Similar Classification Devices (EJH)
Other Devices by PRIMOTEC LLC
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