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Sign in to claim this brandMölnlycke Health Care AB
US
Last updated May 24, 2026
Information
- Country
- US
- Address
- —
- Website
- molnlycke.com
- —
- —
- [email protected]
- Phone
- +46737733775
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- —
- DUNS Number
- 631770658
Catalogue (662)
Page 4 of 14| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Mölnlycke® | 620500 | FDA UDI | Class I | Active |
| Exufiber® | 709905 | FDA UDI | Class I | Active |
| Tubigrip® | 1448 | FDA UDI | Class I | Active |
| Mepilex® Border Flex | 595300 | FDA UDI | Class I | Active |
| Mefix® | 310599 | FDA UDI | Class I | Active |
| Mepilex® Border Post-Op Ag | 498600 | FDA UDI | U | Active |
| Avance® Solo | 8880050 | FDA UDI | Class II | Active |
| Biogel Eclipse® | 75270 | FDA UDI | Class I | Active |
| Biogel PI Indicator® Underglove | 41675 | FDA UDI | Class I | Active |
| Mefix® | 311000 | FDA UDI | Class I | Active |
| Mepilex® Border Sacrum | 282000 | FDA UDI | Class I | Active |
| Exufiber® | 709907 | FDA UDI | Class I | Active |
| Exufiber® Ag+ | 603425 | FDA UDI | U | Active |
| Mepilex® | 294499 | FDA UDI | Class I | Active |
| Avance® Solo | 882525 | FDA UDI | Class II | Active |
| Mepore® | 671200 | FDA UDI | Class I | Active |
| Mepilex® Border Post-Op Ag | 498100 | FDA UDI | U | Active |
| Biogel® PI Micro | 48590 | FDA UDI | Class I | Active |
| Barrier | 42381-01 | FDA UDI | Class II | Active |
| Barrier | 42361-01 | FDA UDI | Class II | Active |
| Mefix® | 310500 | FDA UDI | Class I | Active |
| Mepilex® | 294399 | FDA UDI | Class I | Active |
| Mepore® Film | 350450 | FDA UDI | U | Active |
| Biogel Sensor® | 82560 | FDA UDI | Class I | Active |
| Mepitel® | 292005 | FDA UDI | Class II | Active |
| Mepore® Film | 273000 | FDA UDI | Class I | Active |
| Alldress® | 265329 | FDA UDI | Class I | Active |
| Mepilex® | 294015 | FDA UDI | Class I | Active |
| Mepilex® Border Flex | 595333 | FDA UDI | Class I | Active |
| Biogel® PI UltraTouch® | 42155 | FDA UDI | Class I | Active |
| Mepilex® Border Post-Op Ag | 498300 | FDA UDI | U | Active |
| Biogel PI Indicator® Underglove | 41655 | FDA UDI | Class I | Active |
| Tortoise™ Turning & positioning system | 1400800 | FDA UDI | Class I | Active |
| Biogel® Surgeons | 30485 | FDA UDI | Class I | Active |
| Biogel® PI UltraTouch® S | 45585 | FDA UDI | Class I | Active |
| Tubifast® | 2434 | FDA UDI | Class I | Active |
| Tubigrip® | 1512 | FDA UDI | Class I | Active |
| Avance® Solo | 8881035 | FDA UDI | Class II | Active |
| Mepilex® XT | 211200 | FDA UDI | Class I | Active |
| Biogel® Optifit® Orthopaedic | 31060 | FDA UDI | Class I | Active |
| Tortoise™ Turning & positioning system | 1400800 | FDA UDI | Class I | Active |
| Mepilex® Lite | 284188 | FDA UDI | Class I | Active |
| Tubigrip® | 1547 | FDA UDI | Class I | Active |
| Biogel® PI UltraTouch® S Indicator® System | 45970 | FDA UDI | Class I | Active |
| Avance® Solo | 881030 | FDA UDI | Class II | Active |
| Mepitel® | 290599 | FDA UDI | Class II | Active |
| Mepilex® Border Ag | 395690 | FDA UDI | U | Active |
| Biogel Sensor® | 30670 | FDA UDI | Class I | Active |
| Biogel Sensor® | 82555 | FDA UDI | Class I | Active |
| Mefix® | 311099 | FDA UDI | Class I | Active |
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