moorVMS-VASC PC Software

FDA UDI

Class II (US FDA UDI)

by Moor Instruments Limited

Identity

Trade Name: moorVMS-VASC PC Software FDA UDI
Generic Name: Laser Doppler blood flowmeter FDA UDI
Device Name: Clinical software for micro vascular assessments in physiological research and clinical applications. FDA UDI
Model / Reference: 2 FDA UDI
Description: Clinical software for micro vascular assessments in physiological research and clinical applications. FDA UDI

Identifiers

Primary DI / UDI-DI: 15060484490102 FDA UDI
510(k) Number: K083082 FDA UDI
K102433 FDA UDI
FDA Product Code: DPW FDA UDI
GEX FDA UDI
GMDN Term: Laser Doppler blood flowmeter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.2100 FDA UDI
878.4810 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Laser Doppler blood flowmeter

moorVMS-VASC PC Software by Moor Instruments Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K083082 also covers:

K102433 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Moor Instruments Limited

Sources (1)

FDA UDI 4fe92ca6-fd4b-4531-a7de-048ee6f6c18f 35 fields · synced May 30, 2026