| Primary Device ID | 07323190019687 |
| NIH Device Record Key | 5e25bcab-60f3-4f75-9ef6-7e5748fc0dad |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mepitel® Ag |
| Version Model Number | 390090 |
| 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 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 | 07323190019687 [Package] Contains: 07323190019694 Package: CASE [6 Units] In Commercial Distribution |
| GS1 | 07323190019694 [Package] Contains: 07323190019915 Package: PACK_OR_INNER_PACK [10 Units] In Commercial Distribution |
| GS1 | 07323190019915 [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 |
| 07323190019816 | Mepitel Ag 20x50cm US |
| 07323190019762 | Mepitel Ag 20x30cm US |
| 07323190019731 | Mepitel Ag 10x18 US |
| 07323190019687 | Mepitel Ag 10x12cm US |
| 07323190019656 | Mepitel Ag 7,5x10cm US |
| 07323190019618 | Mepitel Ag 5x7,5cm US |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MEPITEL 73721142 1682605 Live/Registered |
MOLNLYCKE AB 1988-04-05 |