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Breg

FDA UDI

Class II (US FDA UDI)

by Breg, Inc.

Identity

Trade Name
BREG FDA UDI
Generic Name
Inflatable hot/cold therapy pack/electric pump FDA UDI
Model / Reference
NOVAPLUS PAD INTELLI FLO SHOULDER FDA UDI

Identifiers

Catalog Number
V10220 FDA UDI
Primary DI / UDI-DI
00672736140772 FDA UDI
FDA Product Code
ILO FDA UDI
GMDN Term
Inflatable hot/cold therapy pack/electric pump FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5720 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Inflatable hot/cold therapy pack/electric pump

Breg by Breg, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inflatable hot/cold therapy pack/electric pump.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Breg, Inc.

Sources (1)

  • FDA UDI 599e9f8a-9a58-4bd3-9a38-a35b3a2d3a2c 34 fields · synced Jun 6, 2026