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PeriSoft for Windows Examination Manager

FDA UDI

Class II (US FDA UDI)

by Perimed, Inc.

Identity

Trade Name
PeriSoft for Windows Examination Manager FDA UDI
Generic Name
Laser Doppler blood flowmeter FDA UDI
Device Name
PeriSoft for Windows Examination Manager FDA UDI
Model / Reference
PSW ExM FDA UDI
Description
PeriSoft for Windows Examination Manager FDA UDI

Identifiers

Primary DI / UDI-DI
07332834000332 FDA UDI
510(k) Number
K922368 FDA UDI
FDA Product Code
DPW FDA UDI
GMDN Term
Laser Doppler blood flowmeter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.2100 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Laser Doppler blood flowmeterTranscutaneous blood gas monitoring system

PeriSoft for Windows Examination Manager by Perimed, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transcutaneous blood gas monitoring system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Perimed, Inc.

Sources (1)

  • FDA UDI 89a309db-4515-4525-b3ce-24fe1d9ec9e9 34 fields · synced May 29, 2026