Primary Device ID | 00810118103193 |
NIH Device Record Key | 3ee3a332-d073-47d6-ba1f-976e91bfaf3e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NeoLINER LC 1 g Kit (Canada) |
Version Model Number | NNLCSK |
Company DUNS | 185497372 |
Company Name | NUSMILE, LTD. |
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 | true |
Device Combination Product | false |
Single Use | false |
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 |