IOLMATIC injector system

Organization name

Iolution GmbH

SRN

DE-MF-000005687

Manufacturer status

Active

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

• CW011

  EUDAMED did not publish a description for this code.
• CW009

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

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

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

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

  EUDAMED did not publish a description for this code.

Primary placement in Netherlands; available across 32 countries total.

Trade name

IOLMATIC injector system

UDI-DI code

04260676610736

Basic UDI-DI

B-04260676610736

Reference / catalog number

200-12-2.0-A002

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

The single-use IOLMATIC injector system is intended to be used for implantation of qualified foldable intraocular lenses into the eye following cataract removal. Validation of compatibility between IOLMATIC injector system and intraocular lens according to ISO 11979 performed by the lens manufacturer is required for qualification of lens.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• Q021111OCULAR IMPLANT INSTRUMENTS, SINGLE-USE

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