GKS PRIME FLEX: TRIAL FEMUR, Flat Inner, Titanium - Size 5 LEFT

Organization name

Permedica S.p.A

SRN

IT-MF-000008110

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

1 warning recorded — scroll inside the panel to see all entries.

• CW010

  EUDAMED did not publish a description for this code.

Primary placement in Italy; available across 32 countries total.

Trade name

GKS PRIME FLEX: TRIAL FEMUR, Flat Inner, Titanium - Size 5 LEFT

UDI-DI code

08050323151059

Basic UDI-DI

B-08050323151059

Reference / catalog number

S54474

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

MDD [Directive 93/42/EEC 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

• 5 LEFT

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

• V06010102KNEE PROSTHESES TESTING DEVICES