Primary Device ID | 07323190013531 |
NIH Device Record Key | 1029ae9e-d718-4531-8268-8d1cd01fd66a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mepilex® Transfer Ag |
Version Model Number | 394890 |
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 |
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Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07323190013524 [Package] Package: CASE [5 Units] In Commercial Distribution |
GS1 | 07323190013531 [Package] Contains: 07323190018826 Package: PACK_OR_INNER_PACK [10 Units] In Commercial Distribution |
GS1 | 07323190018826 [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 |
07323190013395 | Mepilex Transfer Ag 20x50cm US |
07323190013531 | Mepilex Transfer Ag 15x20cm, US |
07323190013203 | Mepilex Transfer Ag 10x12,5cm US |
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 |