Primary Device ID | 30844509000823 |
NIH Device Record Key | 38c1f9fa-3f77-4fa2-82c5-23e41dc0ce83 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cyto-Chex BCT |
Version Model Number | 213386 |
Catalog Number | 213386 |
Company DUNS | 072915986 |
Company Name | STRECK, INC. |
Device Count | 100 |
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 | 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 |
Phone | 1-800-228-6090 |
custserv@streck.com | |
Phone | 1-800-228-6090 |
custserv@streck.com |
Total Volume | 5 Milliliter |
Total Volume | 5 Milliliter |
Storage Environment Temperature | Between 18 Degrees Celsius and 30 Degrees Celsius |
Storage Environment Temperature | Between 18 Degrees Celsius and 30 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00844509000822 [Unit of Use] |
GS1 | 30844509000823 [Primary] |
GIM | Tubes, Vacuum Sample, With Anticoagulant |
Steralize Prior To Use | false |
Device Is Sterile | true |
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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