moorVMS-PC Software

FDA UDI

Class II (US FDA UDI)

by Moor Instruments Limited

Identity

Trade Name: moorVMS-PC Software FDA UDI
Generic Name: Tissue saturation oximeter FDA UDI
Device Name: moorVMS-PC Software V4.0 is a Windows based software package designed to work with the moorVMS setup and is fully compatible with all of the existing modules. FDA UDI
Model / Reference: 4 FDA UDI
Description: moorVMS-PC Software V4.0 is a Windows based software package designed to work with the moorVMS setup and is fully compatible with all of the existing modules. FDA UDI

Identifiers

Primary DI / UDI-DI: 15060484490096 FDA UDI
510(k) Number: K083082 FDA UDI
K102433 FDA UDI
K112826 FDA UDI
FDA Product Code: MUD FDA UDI
DPW FDA UDI
GEX FDA UDI
GMDN Term: Tissue saturation oximeter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.2700 FDA UDI
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 Tissue saturation oximeter

moorVMS-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:

K112826 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 ddb321f1-cdb3-4b5c-908f-b4b7197a44b5 35 fields · synced May 31, 2026