Primary Device ID | 10887761983455 |
NIH Device Record Key | d1a113ba-f271-4493-9511-4eaa4e27078f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FixStrap™ |
Version Model Number | 3696001 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00887761983458 [Primary] |
GS1 | 10887761983455 [Package] Contains: 00887761983458 Package: [10 Units] In Commercial Distribution |
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 | 2021-03-29 |
Device Publish Date | 2021-03-19 |
10887761983455 | General-purpose patient lifting system sling/harness |
10887761979595 | Patient transfer sliding mat |