Primary Device ID | 00802807150038 |
NIH Device Record Key | 7cc6d062-de63-4dea-8181-34537d7cd84a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | WHIMS |
Version Model Number | 4285 WHIMS |
Company DUNS | 825224459 |
Company Name | Evolutioneyes, Inc. |
Device Count | 3 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00802807150038 [Unit of Use] |
GS1 | 00802807356188 [Primary] |
HOI | Spectacle, magnifying |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-06 |
Device Publish Date | 2023-11-28 |
00802807100101 | READER 3 PACK |
00802807150038 | READER 3 PACK |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
WHIMS 97227833 not registered Live/Pending |
Jesse Barruch Inc. 2022-01-19 |
WHIMS 85707771 4582508 Live/Registered |
Khorram, Ali 2012-08-20 |
WHIMS 85680123 4437322 Live/Registered |
Evolutioneyes, Inc 2012-07-18 |
WHIMS 78227457 3004925 Dead/Cancelled |
PEPPERIDGE FARM, INCORPORATED 2003-03-19 |
WHIMS 74352245 1810573 Dead/Cancelled |
CULLMAN VENTURES INC 1993-01-25 |
WHIMS 73835738 1626417 Dead/Cancelled |
R.N. KOCH, INC. 1989-11-01 |
WHIMS 73510410 not registered Dead/Abandoned |
SYLRAY, INC. 1984-11-23 |
WHIMS 73271672 1172009 Dead/Cancelled |
Klockner-Humboldt-Deutz AG 1980-07-25 |
WHIMS 73250732 1194883 Dead/Cancelled |
Whims, Inc. 1980-02-19 |
WHIMS 71555434 0517471 Dead/Expired |
NORRIS INC. 1948-04-23 |