| Primary Device ID | 05708265000821 |
| NIH Device Record Key | babb0ffb-3c0b-40c2-b7cc-8b4207787982 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | LiNA Skin Hook™ |
| Version Model Number | SH-120 |
| Catalog Number | SH-120 |
| 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 |
| Phone | +48 612222143 |
| info.poland@lina-medical.com | |
| Phone | +48612222121 |
| info.poland@lina-medical.com | |
| Phone | +48612222121 |
| info.poland@lina-medical.com | |
| Phone | +48612222121 |
| info.poland@lina-medical.com | |
| Phone | +48612222121 |
| info.poland@lina-medical.com | |
| Phone | +48612222121 |
| info.poland@lina-medical.com | |
| Phone | +48612222121 |
| info.poland@lina-medical.com | |
| Phone | +48612222121 |
| info.poland@lina-medical.com | |
| Phone | +48612222121 |
| info.poland@lina-medical.com | |
| Phone | +48612222121 |
| info.poland@lina-medical.com | |
| Phone | +48612222121 |
| info.poland@lina-medical.com | |
| Phone | +48612222121 |
| info.poland@lina-medical.com | |
| Phone | +48612222121 |
| info.poland@lina-medical.com | |
| Phone | +48612222121 |
| info.poland@lina-medical.com | |
| Phone | +48612222121 |
| info.poland@lina-medical.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00000000000000 [Unit of Use] |
| GS1 | 05708265000418 [Primary] |
| GS1 | 05708265000821 [Package] Contains: 05708265000418 Package: box [5 Units] In Commercial Distribution |
| GS1 | 05708265012671 [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 |