Primary Device ID | 00887761983441 |
NIH Device Record Key | ff3a213a-ca6e-4350-ae28-b0b2f79f45f3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Liko Solo HighBack Sling™, Mod. 25 |
Version Model Number | 3525917 |
Company DUNS | 354818510 |
Company Name | Liko 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 | false |
Manufacturing Date | false |
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 | false |