022.0031

Trade name

not provided

UDI-DI code

Primary DI

The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.

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07630031727862

Basic UDI-DI

Basic UDI-DI

The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.

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0763003170062QQ

Reference / catalog number

022.0031

Issuing entity

UDI issuing entities

Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.

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GS1

Risk category

MDR risk classes

MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.

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Class IIb

Applicable legislation

MDR [Regulation (EU) 2017/745 on medical devices]

Status

On the market

Quantity

1

Additional product description

RC Pre-milled Abutment Blank, for Medentika Holder, Ø 15.8, TAN

Additional information URL

https://ifu.straumann.com/

Clinical sizes

• 15.8 MU50

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

• P01020101DENTAL IMPLANTS

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

• CW010

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

  EUDAMED did not publish a description for this code.

No certificate specifically references this device's Basic UDI-DI.