eudamed_udi
Primary ID: 08000061079894
My doct - kinesioterapia nera (UDI 08000061079894)
Manufactured by Eurosirel Spa
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for My doct - kinesioterapia nera - Primary ID 08000061079894
Device Regulatory Overview
The My doct - kinesioterapia nera (Model/Catalog Number: BK079894) is a medical device manufactured by Eurosirel Spa. This product is indexed under FDA Product Code / Category Classification Z12069099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BK079894
- Product Code / EMDN
- Z12069099
- Device Name
- BENDA ELASTICA ADESIVA KINETIC
- Database Sync Date
- 2026-08-09 16:28:46
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 My doct - kinesioterapia nera?
The registered manufacturer of record for My doct - kinesioterapia nera is Eurosirel Spa.
What is the Primary UDI-DI identifier for My doct - kinesioterapia nera?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08000061079894.
What classification code is assigned to this device?
This device is registered under product classification code Z12069099.
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