Primary Device ID | 07323190196388 |
NIH Device Record Key | bfb2c988-958d-4cab-bb55-fbc2e512e0ea |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mepore® |
Version Model Number | 670800 |
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 | 07323190196371 [Package] Package: CASE [8 Units] In Commercial Distribution |
GS1 | 07323190196388 [Package] Contains: 07323190198344 Package: PACK_OR_INNER_PACK [60 Units] In Commercial Distribution |
GS1 | 07323190198344 [Primary] |
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 |
07323190254798 | Mepore 10x11 cm |
07323190254705 | Mepore 9x30cm |
07323190254637 | Mepore 9x25cm |
07323190196388 | Mepore 6x7cm |
07323190196418 | Mepore 9x10cm |
07323190254750 | Mepore 9x35cm |
07323190254385 | Mepore 9x15cm OTC Norden |
07332430675125 | Mepore Roll 7cmx5m |
07332430675088 | Mepore Roll 4cmx5m |
07323190254545 | Mepore 9x20cm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MEPORE 79022307 3194683 Live/Registered |
Mölnlycke Health Care AB 2006-02-03 |
MEPORE 75179736 not registered Dead/Abandoned |
SCA Molnlycke AB 1996-10-10 |
MEPORE 74110812 1657995 Live/Registered |
MOLNLYCKE HEALTH CARE AB 1990-10-30 |
MEPORE 73416701 1306759 Dead/Cancelled |
Molnlycke Aktiebolag 1983-03-10 |