CoolCard Max BRZ-CD1-08X-QCK

GUDID 00816417020339

CoolCard Max - Quick Check

Zeltiq Aesthetics, Inc.

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Primary Device ID00816417020339
NIH Device Record Key306d6792-c08d-4aa1-8b8f-2f79d71c783d
Commercial Distribution StatusIn Commercial Distribution
Brand NameCoolCard Max
Version Model NumberBRZ-CD1-08X-QCK
Catalog NumberBRZ-CD1-08X-QCK
Company DUNS809152916
Company NameZeltiq Aesthetics, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone888-935-8471
Emailsupport@zeltiq.com
Phone888-935-8471
Emailsupport@zeltiq.com
Phone888-935-8471
Emailsupport@zeltiq.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100816417020339 [Primary]

FDA Product Code

OOKDermal Cooling Pack/Vacuum/Massager

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-23

On-Brand Devices [CoolCard Max ]

00816417020445CoolCard Max - 16 Cycle
00816417020438CoolCard Max - 8 Cycle
00816417020421CoolCard Max - 3 Cycle
00816417020414CoolCard Max - 1 Cycle
00816417020339CoolCard Max - Quick Check

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