Primary Device ID | 05056341601913 |
NIH Device Record Key | 6c881cf3-5493-4882-ba47-60ab2c282168 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ninjo |
Version Model Number | FA1B021CAUS1 |
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 |