eudamed_udi
Primary ID: 07613427019895
OneTouch Verio Control Solution (UDI 07613427019895)
Manufactured by LifeScan Europe GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OneTouch Verio Control Solution - Primary ID 07613427019895
Device Regulatory Overview
The OneTouch Verio Control Solution (Model/Catalog Number: 022223) is a medical device manufactured by LifeScan Europe GmbH. This product is indexed under FDA Product Code / Category Classification W0101050205 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 022223
- Product Code / EMDN
- W0101050205
- Device Name
- OneTouch Verio Control Solution
- Database Sync Date
- 2026-08-09 17:01:53
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 OneTouch Verio Control Solution?
The registered manufacturer of record for OneTouch Verio Control Solution is LifeScan Europe GmbH.
What is the Primary UDI-DI identifier for OneTouch Verio Control Solution?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07613427019895.
What classification code is assigned to this device?
This device is registered under product classification code W0101050205.
Similar Classification Devices (W0101050205)
Other Devices by LifeScan Europe GmbH
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