LK021

Organization name

Cavex Holland BV

SRN

NL-MF-000000423

Manufacturer status

Active

Certificate health across this manufacturer's portfolio.

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

• CW042

  EUDAMED did not publish a description for this code.
• CW086

  EUDAMED did not publish a description for this code.
• CW044

  EUDAMED did not publish a description for this code.
• CW096

  EUDAMED did not publish a description for this code.
• CW101

  EUDAMED did not publish a description for this code.
• CW045

  EUDAMED did not publish a description for this code.
• CW103

  EUDAMED did not publish a description for this code.
• CW104

  EUDAMED did not publish a description for this code.

Primary placement in Netherlands; available across 15 countries total.

Trade name

not provided

UDI-DI code

E241LK0210

Basic UDI-DI

B-E241LK0210

Reference / catalog number

LK021

Issuing entity

HIBCC

Risk category

Class IIa

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

capsule I spill 50 caps

Additional information URL

https://www.cavex.nl/wp-content/uploads/2022/10/2022-01-IFU-Cavex-Non-Gamma2-ZL709-14-MDD.pdf

Clinical sizes

No clinical sizes registered for this device.

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

E241LK0210

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

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

• Q01010101AMALGAMS FOR RESTORATIVE DENTISTRY