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Conair

FDA UDI

Class I (US FDA UDI)

by Conair Llc.

Identity

Trade Name
CONAIR FDA UDI
Generic Name
External electric-heating core temperature regulation system pad FDA UDI
Device Name
Small Massaging Heating Pad FDA UDI
Model / Reference
HP12 FDA UDI
Description
Small Massaging Heating Pad FDA UDI

Identifiers

Primary DI / UDI-DI
00074108457868 FDA UDI
FDA Product Code
ISA FDA UDI
IRT FDA UDI
GMDN Term
External electric-heating core temperature regulation system pad FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5660 FDA UDI
890.5740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Hand-held electric massagerExternal electric-heating core temperature regulation system pad

Conair by Conair Llc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as External electric-heating core temperature regulation system pad.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conair Llc.

Sources (1)

  • FDA UDI fbfd8b3f-cfef-4f18-939f-4701fe12df5a 33 fields · synced May 30, 2026