H42-508

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-80565185004803G

Basic UDI-DI

B-80565185004803G

Reference / catalog number

H42-508

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

Hydrogel Oral - 5 syr 0.8 cc/syr

Additional information URL

https://bioteck.com/bh42

Clinical sizes

• 0.8 MU12

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

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