266115

Organization name

ACTEON MANUFACTURING

SRN

FR-MF-000007556

Manufacturer status

Active

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

• CW081

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

  EUDAMED did not publish a description for this code.
• CW129

  EUDAMED did not publish a description for this code.
• CW158

  EUDAMED did not publish a description for this code.
• CW162

  EUDAMED did not publish a description for this code.
• CW167

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

  EUDAMED did not publish a description for this code.
• CW194

  EUDAMED did not publish a description for this code.
• CW401

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

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

  EUDAMED did not publish a description for this code.
• CW183

  EUDAMED did not publish a description for this code.

Primary placement in France; available across 14 countries total.

Trade name

not provided

UDI-DI code

03760243000805

Basic UDI-DI

B-03760243000805

Reference / catalog number

266115

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

250 ml bottle in a box with an IFU.

Additional information URL

https://www.acteongroup.com/documentation

Clinical sizes

No clinical sizes registered for this device.

• Q01010299ROOT CANAL FILLING DEVICES - OTHER

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