| Primary Device ID | 07323190278909 |
| NIH Device Record Key | 0c87b979-a128-4d87-bb1f-871da2da260b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mepilex® |
| Version Model Number | 294499 |
| Company DUNS | 631770658 |
| Company Name | Mölnlycke Health Care AB |
| Device Count | 1 |
| DM Exempt | true |
| 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 | false |
| 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 | false |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07323190277193 [Primary] |
| GS1 | 07323190278893 [Package] Package: CASE [4 Units] In Commercial Distribution |
| GS1 | 07323190278909 [Package] Contains: 07323190277193 Package: PACK_OR_INNER_PACK [5 Units] In Commercial Distribution |
| NAC | Dressing, wound, hydrophilic |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-10-31 |
| Device Publish Date | 2022-10-21 |
| 07323190271535 | Mepilex Heel 15x22cm |
| 07323190272389 | Mepilex 20x50cm |
| 07323190271399 | Mepilex Heel 13x20cm |
| 07323190271689 | Mepilex 10x12 cm |
| 07323190278909 | Mepilex 20x20cm, US |
| 07323190272013 | Mepilex 10x20cm |
| 07323190278787 | Mepilex 10x10 cm, US |
| 07323190278848 | Mepilex 15x15cm |
| 07323190271627 | Mepilex 5x5cm |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MEPILEX 77850168 3820862 Live/Registered |
Mölnlycke Health Care AB 2009-10-16 |
![]() MEPILEX 75582163 2346713 Dead/Cancelled |
Molnlycke Health Care AB 1998-11-03 |