Primary Device ID | 00816995020196 |
NIH Device Record Key | b71e8937-942a-4f37-9ed6-34ba1a45ac41 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Liposonix |
Version Model Number | P006145-01 |
Catalog Number | P006145-01 |
Company DUNS | 079999584 |
Company Name | SOLTA MEDICAL |
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 | 00816995020196 [Primary] |
OHV | Focused Ultrasound For Tissue Heat Or Mechanical Cellular Disruption |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-11-05 |
Device Publish Date | 2016-09-23 |
00816995020219 | SYSTEM, WIFI, LIPOSONIX, P2.1.1 |
00816995020202 | ASSEMBLY, HANDPIECE, P2.X |
00816995020196 | HANDPIECE, REPLACEMENT, P2.X |
00816995020189 | TREATMENT KIT, 1.3CM, WORLDWIDE |
00816995020172 | TREATMENT KIT,EXT. USE, 1.3CM, WORLDWIDE |
00816995020158 | CARTRIDGE, REPLACEABLE TREATMENT |
00816995020141 | INSTALLATION KIT, MODEL 2, GENERIC, P2.1 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LIPOSONIX 85633020 4356670 Live/Registered |
LipoSonix, Inc. 2012-05-23 |
LIPOSONIX 76185377 2896037 Live/Registered |
SOLTA MEDICAL, INC. 2000-12-21 |