eudamed_udi
Primary ID: 03760316090092
TENSI+ (UDI 03760316090092)
Manufactured by Telic, S.A.U.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TENSI+ - Primary ID 03760316090092
Device Regulatory Overview
The TENSI+ (Model/Catalog Number: PF0106) is a medical device manufactured by Telic, S.A.U.. This product is indexed under FDA Product Code / Category Classification C020599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PF0106
- Product Code / EMDN
- C020599
- Device Name
- Electro-gel
- Database Sync Date
- 2026-08-09 16:29:53
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 TENSI+?
The registered manufacturer of record for TENSI+ is Telic, S.A.U..
What is the Primary UDI-DI identifier for TENSI+?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03760316090092.
What classification code is assigned to this device?
This device is registered under product classification code C020599.
Similar Classification Devices (C020599)
Other Devices by Telic, S.A.U.
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