Mepilex® Border Flex Lite
GUDID 00050428433713
Mepilex Border Flex Lite 4x5cm, 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| Primary Device ID | 00050428433713 |
| NIH Device Record Key | 6afb83cd-776d-4beb-af22-6aea543f0a81 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mepilex® Border Flex Lite |
| Version Model Number | 581088 |
| 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 |
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 Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00050428433713 [Package] Contains: 07333350914752 Package: PACK_OR_INNER_PACK [3 Units] In Commercial Distribution |
| GS1 | 07333350471569 [Package] Package: CASE [7 Units] In Commercial Distribution |
| GS1 | 07333350914752 [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 | 2023-12-29 |
| Device Publish Date | 2023-12-21 |
On-Brand Devices [Mepilex® Border Flex Lite]
| 07323190249084 | Mepilex Border Flex Lite 15x15cm |
| 07323190249008 | Mepilex Border Flex Lite 5x12,5cm |
| 07333350157418 | Mepilex Border Flex Lite 10x10cm |
| 07333350912772 | Mepilex Border Flex Lite 4x5cm |
| 07333350382476 | Mepilex Border Flex Lite 7,5x7,5cm |
| 07333350551346 | Mepilex Border Flex Lite 10x10cm, OTC US |
| 07333350515904 | Mepilex Border Flex Lite 5x12,5cm, OTC US |
| 07333350399870 | Mepilex Border Flex Lite 4x5cm, OTC US |
| 07333350389048 | Mepilex Border Flex Lite 7,5x7,5cm, OTC US |
| 00050428436332 | Mepilex Border Flex Lite 5x12,5cm, CVS |
| 00050428433713 | Mepilex Border Flex Lite 4x5cm, CVS |
| 00050428250341 | Mepilex Border Flex Lite 7,5x7,5cm, CVS |
| 00050428435939 | Mepilex Border Flex Lite 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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