Primary Device ID | 07323190195411 |
NIH Device Record Key | 09744968-6e7a-48d0-b8c1-5e4fe75ff9b0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mefix® |
Version Model Number | 310599 |
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 | 07323190195404 [Package] Package: CASE [40 Units] In Commercial Distribution |
GS1 | 07323190195411 [Package] Contains: 07323190203345 Package: PACK_OR_INNER_PACK [1 Units] In Commercial Distribution |
GS1 | 07323190203345 [Primary] |
KGX | Tape and bandage, adhesive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-10-31 |
Device Publish Date | 2022-10-21 |
07323190195923 | Mefix 20cm x 10m |
07323190195879 | Mefix 15cm x 10m, US |
07323190195633 | Mefix 10cm x 10m, US |
07323190195411 | Mefix 5cm x 10m, US |
07323190195169 | Mefix 2,5cm x 10m, US |
07323190195190 | Mefix 5cm x 10m |
07323190195695 | Mefix 15cm x 10m |
07323190195091 | Mefix 2,5cm x 10m |
07323190195442 | Mefix 10cm x 10m |
07323190195985 | Mefix 30cm x 10m |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MEFIX 97404506 not registered Live/Pending |
Shenzhen Rolandi Import & Export Trading Co., Ltd. 2022-05-11 |
MEFIX 79021461 3189687 Live/Registered |
Mölnlycke Health Care AB 2006-02-03 |
MEFIX 73318937 1235141 Live/Registered |
Molnlycke AB 1981-07-14 |