Primary Device ID | 17350025911943 |
NIH Device Record Key | a0b5cec3-711d-4ea4-bec2-34e7a5a2e1f0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ICSI Pipette |
Version Model Number | 14326 |
Company DUNS | 631805488 |
Company Name | Vitrolife Sweden AB |
Device Count | 20 |
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 | true |
OTC Over-The-Counter | false |