eudamed_udi
Primary ID: 06945630120114
OneTouch (UDI 06945630120114)
Manufactured by Sterilance Medical (Suzhou) Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for OneTouch - Primary ID 06945630120114
Device Regulatory Overview
The OneTouch (Model/Catalog Number: 024-343) is a medical device manufactured by Sterilance Medical (Suzhou) Inc.. This product is indexed under FDA Product Code / Category Classification V010402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 024-343
- Product Code / EMDN
- V010402
- Device Name
- Disposable Blood Lancets
- Database Sync Date
- 2026-08-09 16:48:11
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?
The registered manufacturer of record for OneTouch is Sterilance Medical (Suzhou) Inc..
What is the Primary UDI-DI identifier for OneTouch?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06945630120114.
What classification code is assigned to this device?
This device is registered under product classification code V010402.
Similar Classification Devices (V010402)
Other Devices by Sterilance Medical (Suzhou) Inc.
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