Primary Device ID | 00817763022602 |
NIH Device Record Key | e8f354ef-7cca-4db7-9e36-a81d9bdf1333 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | First Sign |
Version Model Number | FSCDIP18114 |
Catalog Number | FSCDIP18114 |
Company DUNS | 602085672 |
Company Name | W.H.P.M. INC. |
Device Count | 25 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817763022602 [Unit of Use] |
GS1 | 10817763022609 [Primary] |
DKZ | Enzyme Immunoassay, Amphetamine |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-11-25 |
Device Publish Date | 2022-11-17 |
00841824102552 | DOA 5 in 1 Test Dipcard, 25Pcs/Box Clia Waived AMP/COC/mAMP/MOR/THC |
00817763022602 | DOA 11 in 1 Test Dip Card, 25Pcs/Box; First Sign for Hemosure, CLIA Waived AMP/BARB/BUP/BZO/COC/ |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() FIRST SIGN 87717172 5539396 Live/Registered |
Benchmark Holdings LLC 2017-12-12 |
![]() FIRST SIGN 86497994 4799096 Live/Registered |
W.H.P.M. Inc. 2015-01-07 |
![]() FIRST SIGN 85372380 4293012 Live/Registered |
W.H.P.M., Inc. 2011-07-15 |
![]() FIRST SIGN 77886538 not registered Dead/Abandoned |
John Wan 2009-12-04 |
![]() FIRST SIGN 73092649 1059761 Dead/Cancelled |
J. B. Williams Company, Inc., The 1976-07-07 |
![]() FIRST SIGN 72396265 0939544 Dead/Expired |
J. B. WILLIAMS COMPANY, INC., THE 1971-06-30 |