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Breg

FDA UDI

Class II (US FDA UDI)

by Breg, Inc.

Identity

Trade Name
BREG FDA UDI
Generic Name
Circulating-fluid localized thermal therapy system control unit FDA UDI
Device Name
1 Ice Water Container, 1 6 VDC output and 120 VAC 60 Hz input transformer and 1 04750 WO Hip Polar Pad FDA UDI
Model / Reference
PC GLACIER W/ HIP WO FDA UDI
Description
1 Ice Water Container, 1 6 VDC output and 120 VAC 60 Hz input transformer and 1 04750 WO Hip Polar Pad FDA UDI

Identifiers

Catalog Number
10914 FDA UDI
Primary DI / UDI-DI
00672736031155 FDA UDI
FDA Product Code
ILO FDA UDI
GMDN Term
Circulating-fluid localized thermal therapy system control unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5720 FDA UDI
Commercial Distribution
Not 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

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Breg, Inc.

Sources (1)

  • FDA UDI 8714e500-e4f7-4f43-95b7-e8f6a422c6c7 36 fields · synced May 30, 2026