V-Nd:YAG Spot 5.5 mm VTL44040-2

GUDID 07290016746235

V-Nd:YAG Spot 5.5 mm

VIORA LTD

Laser skin surface treatment system applicator Dermatological laser beam guiding handpiece Dermatological laser beam guiding handpiece Dermatological laser beam guiding handpiece Dermatological laser beam guiding handpiece Dermatological laser beam guiding handpiece Dermatological laser beam guiding handpiece Dermatological laser beam guiding handpiece Dermatological laser beam guiding handpiece Dermatological laser beam guiding handpiece Dermatological laser beam guiding handpiece Dermatological laser beam guiding handpiece
Primary Device ID07290016746235
NIH Device Record Keyc6d8a1ad-6906-4486-9578-64edee820321
Commercial Distribution StatusIn Commercial Distribution
Brand NameV-Nd:YAG Spot 5.5 mm
Version Model NumberVTL44040-2
Catalog NumberVTL44040-2
Company DUNS514612758
Company NameVIORA LTD
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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone8884151192
EmailCustomerCareUSA@vioramed.com
Phone8884151192
EmailCustomerCareUSA@vioramed.com
Phone8884151192
EmailCustomerCareUSA@vioramed.com
Phone8884151192
EmailCustomerCareUSA@vioramed.com
Phone8884151192
EmailCustomerCareUSA@vioramed.com
Phone8884151192
EmailCustomerCareUSA@vioramed.com
Phone8884151192
EmailCustomerCareUSA@vioramed.com
Phone8884151192
EmailCustomerCareUSA@vioramed.com
Phone8884151192
EmailCustomerCareUSA@vioramed.com
Phone8884151192
EmailCustomerCareUSA@vioramed.com
Phone8884151192
EmailCustomerCareUSA@vioramed.com
Phone8884151192
EmailCustomerCareUSA@vioramed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS107290016746235 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEXPowered Laser Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-23

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07290016746068 - V-IPL HP Extended2018-07-06 V-IPL HP Extended
07290016746075 - V-IPL Filter HR-630  2018-07-06 V-IPL Filter HR-630  

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