BGS-22

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.
• CW007

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

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

  COLLAGEN
• 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-80565185093154X

Basic UDI-DI

B-80565185093154X

Reference / catalog number

BGS-22

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

Cancellous granules - 1 btl / 2g 1-2mm

Additional information URL

https://bioteck.com/bbgn

Clinical sizes

• 2 MU24
• 4 MU12
• 1–2 MU50

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

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