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PF 6053 Segmental Pressure 4 Cuff Method Kit

FDA UDI

by Perimed, Inc.

Identity

Trade Name
PF 6053 Segmental Pressure 4 Cuff Method Kit FDA UDI
Generic Name
Laser Doppler blood flowmeter FDA UDI
Device Name
PF 6053 Segmental Pressure 4 Cuff Method Kit FDA UDI
Model / Reference
PF 6053 FDA UDI
Description
PF 6053 Segmental Pressure 4 Cuff Method Kit FDA UDI

Identifiers

Catalog Number
93-00230 FDA UDI
Primary DI / UDI-DI
07332834001131 FDA UDI
510(k) Number
K152930 FDA UDI
GMDN Term
Laser Doppler blood flowmeter FDA UDI

Classification

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

Yes

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 flowmeter

PF 6053 Segmental Pressure 4 Cuff Method Kit by Perimed, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laser Doppler blood flowmeter.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Perimed, Inc.

Sources (1)

  • FDA UDI d679f4d6-81d2-48fb-8f87-429fb27c2a8c 35 fields · synced May 30, 2026