Primary Device ID | B80002041000021 |
NIH Device Record Key | 0dc2132f-5274-430b-bd47-f31c0121d9f1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DRUGS OF ABUSE LEVEL 2 |
Version Model Number | DA 2 S IDC |
Company DUNS | 092519016 |
Company Name | UTAK LABORATORIES, INC. |
Device Count | 1 |
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 | 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 | false |
OTC Over-The-Counter | false |
Phone | +1(888) 882-5522 |
welovecontrol@utak.com | |
Phone | +1(888) 882-5522 |
welovecontrol@utak.com | |
Phone | +1(888) 882-5522 |
welovecontrol@utak.com | |
Phone | +1(888) 882-5522 |
welovecontrol@utak.com | |
Phone | +1(888) 882-5522 |
welovecontrol@utak.com | |
Phone | +1(888) 882-5522 |
welovecontrol@utak.com | |
Phone | +1(888) 882-5522 |
welovecontrol@utak.com | |
Phone | +1(888) 882-5522 |
welovecontrol@utak.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B80002041000020 [Primary] |
HIBCC | B80002041000021 [Package] Contains: B80002041000020 Package: Box [4 Units] In Commercial Distribution |
HIBCC | B80002041000022 [Package] Contains: B80002041000020 Package: Box [5 Units] In Commercial Distribution |
HIBCC | B80002041000023 [Package] Contains: B80002041000020 Package: Box [10 Units] In Commercial Distribution |
HIBCC | B80002041000026 [Package] Contains: B80002041000020 Package: Box [25 Units] In Commercial Distribution |
HIBCC | B80002041000027 [Package] Contains: B80002041000020 Package: Box [50 Units] In Commercial Distribution |
HIBCC | B80002041000028 [Package] Contains: B80002041000020 Package: Box [100 Units] In Commercial Distribution |
LAS | Drug Specific Control Materials |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-06-28 |
Device Publish Date | 2022-06-20 |
B800988195 | Drugs of Abuse Level 2 (WB) |
B80002041000021 | DRUGS OF ABUSE LEVEL 2 |
B800DA2WBFRIDH5 | DRUGS OF ABUSE LEVEL 2 |
B800DAUL2FKA5 | DRUGS OF ABUSE LEVEL 2 |
B800DAOF2FPM5 | DRUGS OF ABUSE LEVEL 2 |
B800DAU2V2FUVMG5 | DRUGS OF ABUSE LEVEL 2 |
B800DAU2FAPS5 | DRUGS OF ABUSE LEVEL 2 |
B800DAU2V2SAPC5 | DRUGS OF ABUSE LEVEL 2 |
B800DAU2FLE5 | DRUGS OF ABUSE LEVEL 2 |
B800DA2SFLLS0 | DRUGS OF ABUSE LEVEL 2 |
B800DOA2SMXOFMMC5 | DRUGS OF ABUSE LEVEL 2 |
B800DAUL2UFVMCI5 | DRUGS OF ABUSE LEVEL 2 |
B800DAU2FMED5 | DRUGS OF ABUSE LEVEL 2 |
B800SMXDAU2FPG5 | DRUGS OF ABUSE LEVEL 2 |
B800DA2SSH5 | DRUGS OF ABUSE LEVEL 2 |
B800DA2V2FWBTDHS5 | DRUGS OF ABUSE LEVEL 2 |
B800DAUQC2FMED5 | DRUGS OF ABUSE LEVEL 2 |
B800SMXDAU2V2FPG5 | DRUGS OF ABUSE LEVEL 2 |
B800DAU2ID5 | DRUGS OF ABUSE LEVEL 2 |
B800DAU2FOSUMC5 | DRUGS OF ABUSE LEVEL 2 |
B800DAU2FOL5 | DRUGS OF ABUSE LEVEL 2 |
B800DAU2FHCMC5 | DRUGS OF ABUSE LEVEL 2 |
B800DAU2V2FAPS5 | DRUGS OF ABUSE LEVEL 2 |
B800DA2V2WBNJSP5 | DRUGS OF ABUSE LEVEL 2 |
B800DAOF2FADX5 | DRUGS OF ABUSE LEVEL 2 |
B800DAU2V2NJSP5 | DRUGS OF ABUSE LEVEL 2 |
B800DOA2I2HEOFFMMC5 | DRUGS OF ABUSE LEVEL 2 |
B800DOA2EXTBUFOFFMMC5 | DRUGS OF ABUSE LEVEL 2 |