Primary Device ID | 07333350902957 |
NIH Device Record Key | 8b0cfaba-668a-4810-8f78-d335f7f58943 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mepilex® Border Post-Op Ag |
Version Model Number | 498650 |
Company DUNS | 631770658 |
Company Name | Mölnlycke Health Care AB |
Device Count | 1 |
DM Exempt | false |
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 Issuing Agency | Device ID |
---|---|
GS1 | 07333350378059 [Package] Contains: 07333350668501 Package: PACK_OR_INNER_PACK [5 Units] In Commercial Distribution |
GS1 | 07333350668501 [Primary] |
GS1 | 07333350902957 [Package] Contains: 07333350378059 Package: CASE [8 Units] In Commercial Distribution |
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 | 2023-06-27 |
Device Publish Date | 2023-06-19 |
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 |