0032337

Organization name

lege artis Pharma GmbH + Co. KG

SRN

DE-MF-000006175

Manufacturer status

Active

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

• CW010

  EUDAMED did not publish a description for this code.
• CW135

  EUDAMED did not publish a description for this code.
• CW318

  EUDAMED did not publish a description for this code.
• CW193

  EUDAMED did not publish a description for this code.
• CW334

  EUDAMED did not publish a description for this code.
• CW397

  EUDAMED did not publish a description for this code.
• CW416

  EUDAMED did not publish a description for this code.
• CW999

  With chlorhexidine and xylitol.
• CW999

  Do not use REMOT implant without respective protective if control over the patient’s swallowing reflex is not guaranteed.
• CW999

  Avoid swallowing.
• CW999

  Contact with the eyes must be avoided.
• CW999

  Contra indication: Treatment is not recommended in the case of known allergies to one of the ingredients of REMOT implant.
• CW132

  The safety data sheet can be downloaded from www.legeartis.de or requested by E-Mail from sicherheitsdatenblaetter@legeartis.de

Primary placement in Germany; available across 2 countries total.

Trade name

not provided

UDI-DI code

111669982929

Basic UDI-DI

B-111669982929

Reference / catalog number

0032337

Issuing entity

IFA

Risk category

Class I

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

No clinical sizes registered for this device.

• Q01010403DENTAL ABRASIVE AND POLISHING MATERIALS

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