Primary Device ID | 00844509001430 |
NIH Device Record Key | c838c47c-55b3-4164-83d2-78128c7cbd74 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CVA |
Version Model Number | 291713 |
Catalog Number | 291713 |
Company DUNS | 072915986 |
Company Name | STRECK, INC. |
Device Count | 1 |
DM Exempt | true |
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 | 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 | 1-800-228-6090 |
custserv@streck.com |
Total Volume | 3 Milliliter |
Storage Environment Temperature | Between 2 Degrees Celsius and 10 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00844509001430 [Primary] |
JPK | Mixture, Hematology Quality Control |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-16 |
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