Primary Device ID | 00887761983731 |
NIH Device Record Key | 50254698-eeb6-4811-a56a-e3552a0d2fa6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Liko HygieneVest HighBack™, Mod. 55 |
Version Model Number | 3555117 |
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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887761983731 [Primary] |
FSA | Lift, patient, non-ac-powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-06-17 |
Device Publish Date | 2020-06-09 |
00887761983731 | Patient lifting system divided leg sling |
00887761983724 | Patient lifting system divided leg sling |
00887761983717 | Patient lifting system divided leg sling |
00887761983700 | Patient lifting system divided leg sling |
00887761983694 | Patient lifting system divided leg sling |
00887761983687 | Patient lifting system divided leg sling |