Primary Device ID | 00859268006220 |
NIH Device Record Key | ec29cfb0-c2fd-4804-b532-3516ba696095 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SPERMCARE Lower Layer - Gradient System |
Version Model Number | 2222-K1 |
Catalog Number | 2222-K1 |
Company DUNS | 190094230 |
Company Name | INVITROCARE, INCORPORATED |
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 | 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 |