Mepilex® Border Flex
- Primary DI
- 07323190204779
- Brand
- Mepilex® Border Flex
- Company
- Mölnlycke Health Care AB
- Model
- 595800
- Device description
- Mepilex Border Flex 10x20cm
- Published
- 2022-10-21
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Sterile
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| NAC | Dressing, wound, hydrophilic |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| NAC | Dressing, Wound, Hydrophilic | General, Plastic Surgery | 1 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 07323190204601 | Package | GS1 | 10 | In Commercial Distribution |
| 07333350456146 | Package | GS1 | 3 | In Commercial Distribution |
| 07323190204779 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 07323190204601 | 07323190204601 | 7323190204601 |
| 07333350456146 | 07333350456146 | 7333350456146 |
| 07323190204779 | 07323190204779 | 7323190204779 |
GMDN Terms#
| Term | Definition |
|---|---|
| Wound-nonadherent dressing, absorbent, non-antimicrobial | A wound covering typically in the form of a multi-layered pad having a material or substance on its skin-contact surface (e.g., silicone gel), or designed to be soaked in saline prior to application, to prevent adherence to the wound bed thereby decreasing wound trauma potential; it does not contain an antimicrobial agent. It is typically used to absorb wound blood/exudates while protecting the wound from external contamination and maintaining a moist internal environment. It may be used as a primary or secondary dressing to treat chronic and postoperative wounds, burns, ulcers, abrasions, cuts, or puncture sites; it is not a dedicated burn dressing. This is a single-use device. |
Device Sizes#
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 |
Contacts#
| Phone | |
|---|---|
| +46737733775 | pedro.lopes@molnlycke.com |
Regulatory Flags#
- DUNS number
- 631770658
- Device count
- 1
- Premarket exempt
- true
- Lot or batch
- true
- Expiration date on label
- true
Other Devices From This Company#
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|---|---|---|---|---|
| 07333350181475 | Mölnlycke®Z-Flo™ Fluidized Positioner | 1400500 | 2026-09-22 | |
| 07333350455873 | Mölnlycke®Z-Flo™ Fluidized Positioner | 1400522 | 2026-09-22 | |
| 07333350647292 | Mölnlycke®Z-Flo™ Fluidized Positioner | 1400513 | 2026-09-22 | |
| 07333350743918 | Mölnlycke®Z-Flo™ Fluidized Positioner | 1400527 | 2026-09-22 | |
| 07333350775360 | Mölnlycke®Z-Flo™ Fluidized Positioner | 1400524 | 2026-09-22 | |
| 07333350030384 | Tubigrip® | 1442 | 2026-09-21 | |
| 07333350102111 | Tubigrip® | 1439 | 2026-09-21 | |
| 07333350341596 | Mepitel® | 290799 | 2026-09-21 | |
| 07333350354831 | Tubigrip® | 1452 | 2026-09-21 | |
| 07333350462161 | Mölnlycke®Z-Flo™ Fluidized Positioner | 1401108 | 2026-09-21 | |
| 07333350472917 | Tubigrip® | 1450 | 2026-09-21 | |
| 07333350529079 | Mölnlycke®Z-Flo™ Fluidized Positioner | 1401105 | 2026-09-21 | |
| 07333350589110 | Tubigrip® | 1434 | 2026-09-21 | |
| 07333350644635 | Tubigrip® | 1437 | 2026-09-21 | |
| 07333350721589 | Tubigrip® | 1435 | 2026-09-21 | |
| 07333350753856 | Tubigrip® | 1448 | 2026-09-21 | |
| 07333350758288 | Tubigrip® | 1438 | 2026-09-21 | |
| 07333350768249 | Mölnlycke®Z-Flo™ Fluidized Positioner | 1401111 | 2026-09-21 | |
| 07333350929640 | Tubigrip® | 1449 | 2026-09-21 | |
| 07333350094850 | Tubigrip® | 1451 | 2026-09-18 |
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