Primary Device ID | 05708265000814 |
NIH Device Record Key | 4d418d77-fbb0-46f2-9efb-9c1abb4763bb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LiNA Skin Hook™ |
Version Model Number | SH-110 |
Catalog Number | SH-110 |
Company DUNS | 305088619 |
Company Name | Lina Medical ApS |
Device Count | 2 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00000000000000 [Unit of Use] |
GS1 | 05708265000401 [Primary] |
GS1 | 05708265000814 [Package] Contains: 05708265000401 Package: box [5 Units] In Commercial Distribution |
GS1 | 05708265012657 [Unit of Use] |
GAD | Retractor |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-04-23 |
Device Publish Date | 2016-09-23 |
05708265000838 | LARGE BLUNT, dual pack |
05708265000821 | SMALL BLUNT, dual pack |
05708265000814 | SMALL SHARP, dual pack |