Primary Device ID | M985CIBDTLF0 |
NIH Device Record Key | 3d4a169c-3a1f-4ee8-8191-74991a348b92 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bowie Dick Type Test |
Version Model Number | ProChem |
Catalog Number | CI-BDTLF |
Company DUNS | 102530326 |
Company Name | MESA LABORATORIES, 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 | 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M985CIBDTLF0 [Primary] |
HIBCC | M985CIBDTLF1 [Package] Package: Pack [20 Units] In Commercial Distribution |
HIBCC | M985CIBDTLF2 [Package] Package: Case [80 Units] In Commercial Distribution |
JOJ | Indicator, Physical/Chemical Sterilization Process |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2021-02-19 |
Device Publish Date | 2016-10-24 |
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