| Primary Device ID | 07323190142507 |
| NIH Device Record Key | 88c8c798-e5fe-41a8-91fd-9c56417d9d2c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mepilex® Border Post-Op Ag |
| Version Model Number | 498450 |
| Company DUNS | 631770658 |
| Company Name | Mölnlycke Health Care AB |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 07323190142507 [Package] Contains: 07323190142514 Package: CASE [7 Units] In Commercial Distribution |
| GS1 | 07323190142514 [Package] Contains: 07323190154616 Package: PACK_OR_INNER_PACK [5 Units] In Commercial Distribution |
| GS1 | 07323190154616 [Primary] |
| FRO | Dressing, wound, drug |
| 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 |
| 07323190142583 | Mepilex Border Post-Op Ag 10x35cm |
| 07323190142545 | Mepilex Border Post-Op Ag 10x30cm |
| 07323190142507 | Mepilex Border Post-Op Ag 10x25cm |
| 07323190142460 | Mepilex Border Post-Op Ag 10x20cm |
| 07323190142422 | Mepilex Border Post-Op Ag 10x15cm |
| 07333350513627 | Mepilex Border Post-Op Ag 10x25cm |
| 07333350902957 | Mepilex Border Post-Op Ag 10x35cm |
| 07333350246792 | Mepilex Border Post-Op Ag 6x8cm |
| 07333350085933 | Mepilex Border Post-Op Ag 10x20cm |
| 07333350561192 | Mepilex Border Post-Op Ag 9x10cm |
| 07333350450526 | Mepilex Border Post-Op Ag 10x15cm |
| 07333350958978 | Mepilex Border Post-Op Ag 10x30cm |
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 |