gudid
Primary ID: 03146693119
Accu-Chek Softclix (UDI 03146693119)
Manufactured by Roche Diabetes Care GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Accu-Chek Softclix - Primary ID 03146693119
Device Regulatory Overview
The Accu-Chek Softclix (Model/Catalog Number: 03146693119) is a medical device manufactured by Roche Diabetes Care GmbH. This product is indexed under FDA Product Code / Category Classification QRK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 03146693119
- Product Code / EMDN
- QRK
- Device Name
- Accu-Chek Softclix Lancet 200 (CND, US)
- Database Sync Date
- 2026-08-09 09:08:48
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 Accu-Chek Softclix?
The registered manufacturer of record for Accu-Chek Softclix is Roche Diabetes Care GmbH.
What is the Primary UDI-DI identifier for Accu-Chek Softclix?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03146693119.
What classification code is assigned to this device?
This device is registered under product classification code QRK.
Similar Classification Devices (QRK)
Other Devices by Roche Diabetes Care GmbH
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