Primary Device ID | 07323190019762 |
NIH Device Record Key | 8b800738-3e34-4c3e-9a69-4f6caca14968 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mepitel® Ag |
Version Model Number | 392090 |
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 | 07323190019762 [Package] Contains: 07323190019779 Package: CASE [6 Units] In Commercial Distribution |
GS1 | 07323190019779 [Package] Contains: 07323190019939 Package: PACK_OR_INNER_PACK [5 Units] In Commercial Distribution |
GS1 | 07323190019939 [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 |