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Moor Instruments Ltd

FDA UDI

Class II (US FDA UDI)

by Moor Instruments Limited

Identity

Trade Name
Moor Instruments Ltd FDA UDI
Generic Name
Cutaneous microcirculation laser Doppler imaging device FDA UDI
Device Name
moorLDLS - Laser Doppler Line Scanner FDA UDI
Model / Reference
moorLDLS FDA UDI
Description
moorLDLS - Laser Doppler Line Scanner FDA UDI

Identifiers

Primary DI / UDI-DI
15060484490065 FDA UDI
510(k) Number
K063561 FDA UDI
FDA Product Code
DPT FDA UDI
GMDN Term
Cutaneous microcirculation laser Doppler imaging device FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2120 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

Yes

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

Yes

FDA UDI

Category: Cutaneous microcirculation laser Doppler imaging device

Moor Instruments Ltd by Moor Instruments Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cutaneous microcirculation laser Doppler imaging device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Moor Instruments Limited

Sources (1)

  • FDA UDI dff80b72-56f1-4ccf-b521-65214e3c5d0f 36 fields · synced Jun 1, 2026