ACT-GEL005

Organization name

BIOTECK S.p.A.

SRN

IT-MF-000011484

Manufacturer status

Active

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

• CW010

  EUDAMED did not publish a description for this code.
• CW267

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

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

  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.
• CW129

  EUDAMED did not publish a description for this code.
• CW161

  EUDAMED did not publish a description for this code.

Primary placement in Italy; available across 1 country total.

Trade name

not provided

UDI-DI code

D-80565185020883S

Basic UDI-DI

B-80565185020883S

Reference / catalog number

ACT-GEL005

Issuing entity

EUDAMED

Risk category

Class III

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

DBM Gel - 1 pc / 0.5 cc

Additional information URL

https://bioteck.com/bact

Clinical sizes

• 0.5 MU12

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

• P900401BONE AND TENDON REPLACEMENT DEVICES
• P900402RESORBABLE FILLING AND RECONSTRUCTION DEVICES