MatriDerm

Organization name

Medskin Solutions Dr. Suwelack AG

SRN

DE-MF-000007747

Manufacturer status

Active

8 warnings recorded — scroll inside the panel to see all entries.

• CW010

  EUDAMED did not publish a description for this code.
• CW267

  Treatment with MatriDerm is contraindicated in patients with known hypersensitivity to bovine collagen or elastin
• CW009

  EUDAMED did not publish a description for this code.
• CW001

  EUDAMED did not publish a description for this code.
• CW007

  EUDAMED did not publish a description for this code.
• CW032

  EUDAMED did not publish a description for this code.
• CW999

  The product must not be used in infected wounds!
• CW999

  No clinical data are available concerning the use of MatriDerm in pregnancy and during breastfeeding. Hence, the surgeon’s decision to use MatriDerm must be based on consideration of all the risks in the particular case

Primary placement in Germany; available across 19 countries total.

Trade name

MatriDerm

UDI-DI code

04250569301469

Basic UDI-DI

B-04250569301469

Reference / catalog number

83462-200

Issuing entity

GS1

Risk category

Class III

Applicable legislation

MDD [Directive 93/42/EEC on medical devices]

Status

On the market

Quantity

1

Additional product description

Collagen-Elastin Template

Additional information URL

https://matriderm.com/en

Clinical sizes

No clinical sizes registered for this device.

• P900404AUTOLOGOUS GRAFT SUPPORTS

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

Certificate health across this manufacturer's portfolio.