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MatriDerm, product family

by MedSkin Solutions Dr. Suwelack AG 15 variants Basic UDI-DI 42505690104T

Shared by every variant

Manufacturer
MedSkin Solutions Dr. Suwelack AG(15)
Basic UDI-DI
42505690104T
Risk class
Class III
Legislation
MDDMDR (varies)
EMDN category
AUTOLOGOUS GRAFT SUPPORTS
Market status
13 on the market2 not intended for the eu market
Official record
EUDAMED public site — Open the EUDAMED public site, choose Devices, and search for the Basic UDI-DI 42505690104T.

Certificates

1 certificate naming this Basic UDI-DI · EUDAMED

  • 11830GB450260817 Technical documentation · refdata.applicable-legislation.mdr cancelled
    Notified body 0482 · holder Medskin Solutions Dr. Suwelack AG · issued 17 Aug 2026 · expires 21 Jan 2031

Recalls

0 recalls · FDA

No recall matched the devices on this page.

Recalls matched to the 15 devices listed on this page; other pages of the family can carry others.

Variants

15 devices · page 1 of 1

Variants of MatriDerm, Basic UDI-DI 42505690104T
UDI-DISize and differences
MatriDerm 83400-200 / MatriDerm04250569300080 —On the market
MatriDerm 83401-200 / MatriDerm04250569300059 —On the market
MatriDerm 83403-200 / MatriDerm04250569300035 —On the market
MatriDerm 83411-200 / MatriDerm04250569301292 —On the market
MatriDerm 83413-200 / MatriDerm04250569301315 —On the market
MatriDerm 83421-200 / MatriDerm04250569301339 —On the market
MatriDerm 83423-200 / MatriDerm04250569301353 —On the market
MatriDerm 83441-200 / MatriDerm04250569301414 —On the market
MatriDerm 83443-200 / MatriDerm04250569301438 —On the market
MatriDerm 83461-200 / MatriDerm04250569301452 —On the market
MatriDerm 83462-200 / MatriDerm04250569301469 —On the market
MatriDerm 83470-200 / MatriDerm04250569301483 —On the market
MatriDerm 83500-200 / MatriDerm04250569300073 —On the market
MatriDerm Fenestrated Dermal Matrix 83422-20004250569301346 —Not intended for the EU market
MatriDerm Flex Dermal Matrix 83471-20004250569301490 —Not intended for the EU market