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Duet™

FDA UDI

Class II (US FDA UDI)

by Bio-View Ltd

Identity

Trade Name
Duet™ FDA UDI
Generic Name
Fluorescence light microscope FDA UDI
Model / Reference
Accord Plus FDA UDI

Identifiers

Primary DI / UDI-DI
07290107652780 FDA UDI
FDA Product Code
NTH FDA UDI
GMDN Term
Fluorescence light microscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.4700 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Fluorescence light microscope

Duet™ by Bio-View Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluorescence light microscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bio-View Ltd

Sources (1)

  • FDA UDI 5e819dac-59ba-41b9-96ff-a2019a7874d6 33 fields · synced May 30, 2026