Mepilex® Border Flex
GUDID 00050428358238
Mepilex Border Flex 7,8x10cm, Oval, CVS
Mölnlycke Health Care AB
Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial Wound-nonadherent dressing, absorbent, non-antimicrobial| Primary Device ID | 00050428358238 |
| NIH Device Record Key | 8890cd12-3504-453d-a57b-8b6e8be3eb75 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mepilex® Border Flex |
| Version Model Number | 583588 |
| Company DUNS | 631770658 |
| Company Name | Mölnlycke Health Care AB |
| Device Count | 1 |
| DM Exempt | false |
| 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 |
Customer Support Contacts
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com | |
| Phone | +46737733775 |
| pedro.lopes@molnlycke.com |
Device Dimensions
| 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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00050428358238 [Package] Contains: 07333350796464 Package: PACK_OR_INNER_PACK [3 Units] In Commercial Distribution |
| GS1 | 07333350320454 [Package] Package: CASE [10 Units] In Commercial Distribution |
| GS1 | 07333350796464 [Primary] |
FDA Product Code
| NAC | Dressing, wound, hydrophilic |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-01-29 |
| Device Publish Date | 2024-01-19 |
On-Brand Devices [Mepilex® Border Flex]
| 07323190183128 | Mepilex Border Flex 3,1x4in/7,8x10cm, CVS |
| 07333350798796 | Mepilex Border Flex 7,5x7,5cm |
| 07323190233380 | Mepilex Border Flex 15x19cm, Oval |
| 07323190233342 | Mepilex Border Flex 13x16cm, Oval |
| 07323190233298 | Mepilex Border Flex 7,8x10cm, Oval |
| 07323190298907 | Mepilex Border Comfort 10x30cm |
| 07323190204977 | Mepilex Border Comfort 7.5x7.5cm BRU |
| 07323190298860 | Mepilex Border Flex 10x30cm, FR HC |
| 07323190204526 | Mepilex Border Comfort 15x15cm |
| 07323190204472 | Mepilex Border Comfort 12,5x12,5cm |
| 07323190204441 | Mepilex Border Comfort 10x10cm |
| 07323190204601 | Mepilex Border Flex 10x20cm |
| 07323190173945 | Mepilex Border Flex 15x15 5pack BRU |
| 07333350256623 | Mepilex Border Flex 10x10 cm 5pack BRU |
| 07333350412920 | Mepilex Border Flex 7.5x7.5 10pack BRU |
| 07323190174454 | Mepilex Border Flex 15x20cm |
| 07323190174379 | Mepilex Border Flex 15x15cm |
| 07333350746667 | Mepilex Border Flex 12,5x12,5cm |
| 07333350089757 | Mepilex Border Flex 10x10cm, OTC US |
| 00050428358238 | Mepilex Border Flex 7,8x10cm, Oval, CVS |
| 07333350516123 | Mepilex Border Flex 10x10cm, CVS |
Trademark Results [Mepilex]
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 |
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