Primary Device ID | 70845357034891 |
NIH Device Record Key | 683aa0f6-4264-4033-8cf4-6592e8bc463d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | QC Sets and Panels: KWIK-STIK™ 2 Pack |
Version Model Number | 5215P |
Catalog Number | 5215P |
Company DUNS | 060467826 |
Company Name | MICROBIOLOGICS 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 | 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 |
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70845357039940 | QC Sets and Panels: KWIK-STIK™ Gram Positive Identification Panel |
70845357039933 | QC Sets and Panels: KWIK-STIK™ Gram Negative Identification Panel |
70845357039926 | QC Sets and Panels: KWIK-STIK™ Anaerobe Identification Panel |
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70845357034891 | QC Sets and Panels: KWIK-STIK™ GP Streamlined QC Set |
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70845357030688 | QC Sets and Panels: KWIK-STIK™ GN Comprehensive QC Set |
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