Primary Device ID | 00817766020131 |
NIH Device Record Key | 1b2e3fba-e8e2-4969-9487-a3bd7cfd45ba |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Instrument Cassettes |
Version Model Number | 12 Position Slotted Instrument Cassette |
Catalog Number | 7-1200 |
Company DUNS | 118087931 |
Company Name | Tecomet |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |