Primary Device ID | 07290016541564 |
NIH Device Record Key | 7bc50d22-3f30-4e5c-acea-e41f9ab4688d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BODY LASER APPLICATOR SERVICE PACK, Bliss |
Version Model Number | SPK160000 |
Company DUNS | 533127663 |
Company Name | VENUS CONCEPT LTD |
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 | false |
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 | 07290016541564 [Primary] |
PKT | Laser For Disruption Of Adipocyte Cells For Aesthetic Use |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-07-22 |
Device Publish Date | 2021-07-14 |
07290016541632 - BLISS SYSTEM | 2021-07-22 The Venus Bliss device is a diode laser system intended for non-invasive lipolysis of the abdomen and flanks in individuals with |
07290016541564 - BODY LASER APPLICATOR SERVICE PACK, Bliss | 2021-07-22 |
07290016541564 - BODY LASER APPLICATOR SERVICE PACK, Bliss | 2021-07-22 |
07290016541618 - (MP)2 APPLICATOR BLISS | 2021-07-22 |
07290016541625 - BODY LASER APPLICATOR BLISS | 2021-07-22 |
07290016541717 - (MP)2 APPLICATOR SERVICE PACK, Bliss | 2021-07-22 |
07290016541724 - Belt Bliss | 2021-07-22 |
07290016541984 - Epileve Applicator Service Pack UDI Label | 2021-07-22 The Venus Epileve is intended for all Fitzpatrick skin types, including tanned skin, for use in dermatology, general and plastic |
27290016541179 - HR 690XL Light Block package | 2020-05-01 |