Primary Device ID | 05056097340586 |
NIH Device Record Key | d5c5eaf3-98b0-4650-a49a-dd408fb16ecb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ninjo |
Version Model Number | FA0B011LAUS1 |
Company DUNS | 355804758 |
Company Name | Arjohuntleigh AB |
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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
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 | true |