Primary Device ID | 00817495023069 |
NIH Device Record Key | c4b3bb54-74f2-468c-a1ec-34e0125ae99c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GentleMax Pro Plus |
Version Model Number | 7123-00-0651 |
Company DUNS | 053468385 |
Company Name | CANDELA CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817495023069 [Primary] |
GEX | Powered Laser Surgical Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-30 |
Device Publish Date | 2022-05-20 |
00817495023083 | ASSY, FIBER, STANDARD, HC, GMPP |
00817495023076 | GMPP DCD Large Spot Option Kit, w/HP, w/SAs, w/Fiber Assembly |
00817495023069 | GMPP ACC HP AIR CLIP Kit, w/o Fiber Assembly |
00817495023052 | GMPP DCD Small Spot Option Kit, w/Fiber Assembly |
00817495023045 | GMPP ACC Medium Spot Option Kit, w/Fiber Assembly |
00817495023038 | GMPP ACC Medium Spot Option Kit, w/Fiber Assembly |
00817495023021 | ASSY, DCD HAND PIECE, SMALL SPOT, GMPP |
00817495022994 | ASSY, ACC HAND PIECE, MEDIUM SPOT, GMPP |
00817495022970 | GMPP with PPP |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GENTLEMAX PRO PLUS 90168154 not registered Live/Pending |
Candela Corporation 2020-09-09 |