DE-RQ2233KSM

Organization name

TERUMO EUROPE N.V.

SRN

BE-MF-000001434

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

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

• CW009

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

  EUDAMED did not publish a description for this code.
• CW010

  EUDAMED did not publish a description for this code.
• CW026

  EUDAMED did not publish a description for this code.

Primary placement in Belgium; available across 31 countries total.

Trade name

not provided

UDI-DI code

05413206221158

Basic UDI-DI

5413206UMTCS

Reference / catalog number

DE-RQ2233KSM

Issuing entity

GS1

Risk category

Class III

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 33 MU50
• 2.25 MU50

European Medical Device Nomenclature — the EU product classification assigned to this device.

• P070402010301CORONARY DRUG ELUTING STENTS (DES) WITH POLYMERS