eudamed_udi
Primary ID: 07613427007151
OneTouch Ultra Plus test strip (UDI 07613427007151)
Manufactured by LifeScan Europe GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OneTouch Ultra Plus test strip - Primary ID 07613427007151
Device Regulatory Overview
The OneTouch Ultra Plus test strip (Model/Catalog Number: 023847) is a medical device manufactured by LifeScan Europe GmbH. This product is indexed under FDA Product Code / Category Classification W0101060101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 023847
- Product Code / EMDN
- W0101060101
- Device Name
- OneTouch Ultra Plus test strip
- Database Sync Date
- 2026-08-09 16:28:47
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 Ultra Plus test strip?
The registered manufacturer of record for OneTouch Ultra Plus test strip is LifeScan Europe GmbH.
What is the Primary UDI-DI identifier for OneTouch Ultra Plus test strip?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07613427007151.
What classification code is assigned to this device?
This device is registered under product classification code W0101060101.
Similar Classification Devices (W0101060101)
Other Devices by LifeScan Europe GmbH
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