eudamed_udi
Primary ID: 05060073970520
Kegel8® MultiTone (UDI 05060073970520)
Manufactured by Verity Medical Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kegel8® MultiTone - Primary ID 05060073970520
Device Regulatory Overview
The Kegel8® MultiTone (Model/Catalog Number: OPH120P) is a medical device manufactured by Verity Medical Ltd.. This product is indexed under FDA Product Code / Category Classification Z12062899 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- OPH120P
- Product Code / EMDN
- Z12062899
- Device Name
- Neuromuscular Electrical stimulator system with EMG of physiotherapy, battery powered
- Database Sync Date
- 2026-08-09 17:46:17
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 Kegel8® MultiTone?
The registered manufacturer of record for Kegel8® MultiTone is Verity Medical Ltd..
What is the Primary UDI-DI identifier for Kegel8® MultiTone?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060073970520.
What classification code is assigned to this device?
This device is registered under product classification code Z12062899.
Similar Classification Devices (Z12062899)
Other Devices by Verity Medical Ltd.
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