eudamed_udi
Primary ID: 08720299476301
Anika (UDI 08720299476301)
Manufactured by OOO NPF "Rehabilitation technologies"
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Anika - Primary ID 08720299476301
Device Regulatory Overview
The Anika (Model/Catalog Number: 3) is a medical device manufactured by OOO NPF "Rehabilitation technologies". This product is indexed under FDA Product Code / Category Classification Z12062402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3
- Product Code / EMDN
- Z12062402
- Device Name
- The Anika Complex for Musculoskeletal System Rehabilitation with Biofeedback
- Database Sync Date
- 2026-08-09 18:33:30
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 Anika?
The registered manufacturer of record for Anika is OOO NPF "Rehabilitation technologies".
What is the Primary UDI-DI identifier for Anika?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08720299476301.
What classification code is assigned to this device?
This device is registered under product classification code Z12062402.
Similar Classification Devices (Z12062402)
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