gudid
Primary ID: INSTRUMENT FLUENT 480 BASE UNIT
Fluent (UDI INSTRUMENT FLUENT 480 BASE UNIT)
Manufactured by Tecan Schweiz AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Fluent - Primary ID INSTRUMENT FLUENT 480 BASE UNIT
Device Regulatory Overview
The Fluent (Model/Catalog Number: INSTRUMENT FLUENT 480 BASE UNIT) is a medical device manufactured by Tecan Schweiz AG. This product is indexed under FDA Product Code / Category Classification JQW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- INSTRUMENT FLUENT 480 BASE UNIT
- Product Code / EMDN
- JQW
- Device Name
- configurable liquid handling workstation
- Database Sync Date
- 2026-08-09 09:16:13
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 Fluent?
The registered manufacturer of record for Fluent is Tecan Schweiz AG.
What is the Primary UDI-DI identifier for Fluent?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is INSTRUMENT FLUENT 480 BASE UNIT.
What classification code is assigned to this device?
This device is registered under product classification code JQW.
Similar Classification Devices (JQW)
Other Devices by Tecan Schweiz AG
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