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Pm-750

FDA UDI

Class I (US FDA UDI)

by Pro Medical Supplies, Inc.

Identity

Trade Name
PM-750 FDA UDI
Generic Name
Hand-held electric massager FDA UDI
Device Name
(1) -Infrared Massager Heating Device with Auto Shut-Off - Light Bulb is Included FDA UDI
Model / Reference
PM-750 FDA UDI
Description
(1) -Infrared Massager Heating Device with Auto Shut-Off - Light Bulb is Included FDA UDI

Identifiers

Catalog Number
PM-750 FDA UDI
Primary DI / UDI-DI
00185098000856 FDA UDI
FDA Product Code
ISA FDA UDI
GMDN Term
Hand-held electric massager FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5660 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

Yes

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Hand-held electric massager

Pm-750 by Pro Medical Supplies, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held electric massager.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f679d861-b14b-4c50-a453-d9a19ac98b6f 35 fields · synced May 30, 2026