Mepilex® Border Sacrum
GUDID 07323190176748
Mepilex Border Sacrum 16x20cm BRU
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 | 07323190176748 |
| NIH Device Record Key | 0ec55a93-98db-4093-b706-902b61f8ece4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mepilex® Border Sacrum |
| Version Model Number | 282055 |
| 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 | 07323190176731 [Package] Package: CASE [5 Units] In Commercial Distribution |
| GS1 | 07323190176748 [Package] Contains: 07323190176755 Package: PACK_OR_INNER_PACK [10 Units] In Commercial Distribution |
| GS1 | 07323190176755 [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 | 2023-02-27 |
| Device Publish Date | 2023-02-18 |
On-Brand Devices [Mepilex® Border Sacrum]
| 07332430940612 | Mepilex Border Sacrum 23x23 cm |
| 07332430940599 | Mepilex Border Sacrum 20x20cm |
| 07332430940551 | Mepilex Border Sacrum 18x18 |
| 07323190184170 | Mepilex Border Heel 22x23cm |
| 07323190038381 | Mepilex Border Heel 18,5x24 cm |
| 07323190176700 | Mepilex Border Sacrum 22 x 25 cm BRU |
| 07323190176748 | Mepilex Border Sacrum 16x20cm BRU |
| 07333350834074 | Mepilex Border Sacrum, US 22 x 25 cm |
| 07333350392451 | Mepilex Border Sacrum, US 16x20cm |
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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