CEREFORM®

Organization name

Euromi Biosciences

SRN

BE-MF-000020089

Manufacturer status

Active

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

• CW999

  Non-pyrogenic
• CW999

  Sterile/Sterilised using dry heat - Double sterile barrier system
• CW032

  EUDAMED did not publish a description for this code.
• CW011

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

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

  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 France; available across 11 countries total.

Trade name

CEREFORM®

UDI-DI code

03664685006817

Basic UDI-DI

B-03664685006817

Reference / catalog number

RLS240

Issuing entity

GS1

Risk category

Class III

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

CEREFORM ROUND LOW SMOOTH 240 CLASSIC

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

• 240 MU12

• P0601010202BREAST IMPLANTS, ROUND, MADE OF SILICONE, WITH TEXTURED SURFACE

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