eudamed_udi
Primary ID: 07350012440176
TetraSens Electrode (UDI 07350012440176)
Manufactured by Senzime AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TetraSens Electrode - Primary ID 07350012440176
Device Regulatory Overview
The TetraSens Electrode (Model/Catalog Number: SEN 2012) is a medical device manufactured by Senzime AB. This product is indexed under FDA Product Code / Category Classification Z12062899 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SEN 2012
- Product Code / EMDN
- Z12062899
- Device Name
- TetraSens
- Database Sync Date
- 2026-08-09 16:30:18
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 TetraSens Electrode?
The registered manufacturer of record for TetraSens Electrode is Senzime AB.
What is the Primary UDI-DI identifier for TetraSens Electrode?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07350012440176.
What classification code is assigned to this device?
This device is registered under product classification code Z12062899.
Similar Classification Devices (Z12062899)
Other Devices by Senzime AB
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