Primary Device ID | G6192111211 |
NIH Device Record Key | fd4db477-a164-4714-9d14-4de06f0dfb9c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | COSMEDICO |
Version Model Number | M 650W SE GY9.5 |
Catalog Number | 21112-1 |
Company DUNS | 039280558 |
Company Name | JW NORTH AMERICA, INC. |
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 | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B5331142110 [Previous] |
HIBCC | G6192111210 [Primary] |
HIBCC | G6192111211 [Package] Contains: G6192111210 Package: carton box [25 Units] In Commercial Distribution |
LEJ | Booth, Sun Tan |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-09 |
Device Publish Date | 2024-08-01 |
G6192402211 | Ultraviolet tanning device |
G6192400811 | Ultraviolet tanning device |
G6192400711 | Ultraviolet tanning device |
G6192400611 | Ultraviolet tanning device |
G6192400311 | Ultraviolet tanning device |
G6192111211 | Ultraviolet tanning device |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
COSMEDICO 85495326 4189923 Live/Registered |
JW NORTH AMERICA INC. 2011-12-14 |
COSMEDICO 74479062 1992299 Dead/Cancelled |
COSMEDICO LIGHT, INC. 1994-01-14 |