| Primary Device ID | 04052199273709 |
| NIH Device Record Key | 54aa1ce2-b7fa-49dc-9d0d-2e2ced5463a6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | HydroTac transp. comf. 6,5x10cm st P10 |
| Version Model Number | 685928 |
| Company DUNS | 315768788 |
| Company Name | PAUL HARTMANN AG |
| 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 | 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 | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04052199273686 [Primary] |
| GS1 | 04052199273693 [Package] Contains: 04052199273686 Package: [10 Units] In Commercial Distribution |
| GS1 | 04052199273709 [Package] Contains: 04052199273686 Package: [8 Units] In Commercial Distribution |
| NAD | Dressing, Wound, Occlusive |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-09-09 |
| Device Publish Date | 2020-09-01 |
| 04052199273709 | HydroTac transp. comf. 6,5x10cm st P10 |
| 04049500835138 | HydroTac transp. comf. 6,5x10cm st P10 |