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CoolMini Liner

FDA UDI

Class II (US FDA UDI)

by Zeltiq Aesthetics, Inc.

Identity

Trade Name
CoolMini Liner FDA UDI
Generic Name
Cryolipolysis body contouring system applicator liner FDA UDI
Device Name
CoolMini Liner FDA UDI
Model / Reference
BRZ-LN1-02X-024 FDA UDI
Description
CoolMini Liner FDA UDI

Identifiers

Catalog Number
BRZ-LN1-02X-024 FDA UDI
Primary DI / UDI-DI
10816417020084 FDA UDI
FDA Product Code
OOK FDA UDI
GMDN Term
Cryolipolysis body contouring system applicator liner FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4340 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cryolipolysis body contouring system applicator liner

CoolMini Liner by Zeltiq Aesthetics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cryolipolysis body contouring system applicator liner.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Zeltiq Aesthetics, Inc.

Sources (1)

  • FDA UDI 7d704e48-1b4f-406a-8d8c-5e7df604a73a 35 fields · synced Jun 8, 2026