gudid
Primary ID: 3183807190
Uric Acid ver.2 (UDI 3183807190)
Manufactured by Roche Diagnostics GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Uric Acid ver.2 - Primary ID 3183807190
Device Regulatory Overview
The Uric Acid ver.2 (Model/Catalog Number: 3183807190) is a medical device manufactured by Roche Diagnostics GmbH. This product is indexed under FDA Product Code / Category Classification KNK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3183807190
- Product Code / EMDN
- KNK
- Device Name
- Database Sync Date
- 2026-08-09 09:33:50
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 Uric Acid ver.2?
The registered manufacturer of record for Uric Acid ver.2 is Roche Diagnostics GmbH.
What is the Primary UDI-DI identifier for Uric Acid ver.2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3183807190.
What classification code is assigned to this device?
This device is registered under product classification code KNK.
Similar Classification Devices (KNK)
Other Devices by Roche Diagnostics GmbH
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