5003022XLST

Organization name

Mikai s.p.a.

SRN

IT-MF-000030732

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

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

• CW010

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

Primary placement in Italy; available across 9 countries total.

Trade name

not provided

UDI-DI code

08055731433636

Basic UDI-DI

805573143BSS000HEADLESSGN

Reference / catalog number

5003022XLST

Issuing entity

GS1

Risk category

Class IIb

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

—

Additional information URL

https://www.mikai.us/downloads/

Clinical sizes

No clinical sizes registered for this device.

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

• P09120603CANNULATED SCREWS