Fiber Cable Assembly 7122-20-3141

GUDID 00817495021966

Fiber Assembly

CANDELA CORPORATION

Dermatological laser beam guiding handpiece
Primary Device ID00817495021966
NIH Device Record Key6fd0ba0d-4658-41d3-8e1f-cd144cea3f2e
Commercial Distribution StatusIn Commercial Distribution
Brand NameFiber Cable Assembly
Version Model Number7122-20-3141
Catalog Number7122-20-3141
Company DUNS053468385
Company NameCANDELA CORPORATION
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

Device Identifiers

Device Issuing AgencyDevice ID
GS100817495021966 [Primary]
GS108174950201960 [Previous]

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 Number5
Public Version Date2021-05-24
Device Publish Date2016-10-03

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00817495021959Fiber Assembly

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