| Primary Device ID | 04052199708959 |
| NIH Device Record Key | 8417e3fb-8a14-4dd7-a5bf-391d124acbf9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Zetuvit Plus |
| Version Model Number | 413739 Zetuvit Plus 20 x 60 cm P10 |
| Catalog Number | 413739 |
| 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 | false |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04052199708942 [Primary] |
| GS1 | 04052199708959 [Package] Contains: 04052199708942 Package: FBX [10 Units] In Commercial Distribution |
| GS1 | 04052199740058 [Package] Package: CS [2 Units] In Commercial Distribution |
| NAC | Dressing, Wound, Hydrophilic |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2026-01-21 |
| Device Publish Date | 2024-12-10 |
| 04052199708959 | 413739 Zetuvit Plus 20 x 60 cm P10 |
| 04052199708935 | 413729 Zetuvit Plus 6 x 6 cm P10 |
| 04052199777436 | 413602 Zetuvit Plus Shapes Multisite P10 C6 |
| 04052199777412 | 413601 Zetuvit Plus Shapes Heart Multisite P10 C6 |
| 04052199777382 | 413600 Zetuvit Plus Shapes Oval |