EUDAMED last updated this device on Aug 27, 2026

Titanium cap

40997970004502000000000JQ

On the marketClass IIa

Applicable legislation: —
Organization name: ALTATEC GmbH
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 04099797010947
Reference / catalog number: J2259.6022

Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.

Titanium cap is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by ALTATEC GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: Titanium cap
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 04099797010947
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. View in glossary →: 40997970004502000000000JQ
Reference / catalog number: J2259.6022
UDI issuing entities Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system. View in glossary →: GS1

Classification

Risk category: Class IIa
Applicable legislation: —
Status: On the market

Device details

Quantity: 1
Additional product description: Titanium cap witho. ret. for bar abut., for bridge, 5.0/6.0 mm
Additional information URL: https://ifu.camlog.com/
Clinical sizes: 5–6 MU50

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)04099797010947

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

EMDN nomenclature code(s)

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

P01020180DENTAL IMPLANTS - ACCESSORIES

Critical warnings

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

Consult instructions for use
Caution
Do not re-use
Do not use if package is damaged

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in Germany; available across 24 countries total.

Country	On market since	Until
GermanyPrimary placement	May 20, 2020	Still on market
Austria	May 20, 2020	Still on market
Belgium	May 20, 2020	Still on market
Bulgaria	May 20, 2020	Still on market
Czechia	May 20, 2020	Still on market
Denmark	May 20, 2020	Still on market
EL	May 20, 2020	Still on market
Spain	May 20, 2020	Still on market
Finland	May 20, 2020	Still on market
France	May 20, 2020	Still on market
Croatia	May 20, 2020	Still on market
Hungary	May 20, 2020	Still on market
Ireland	May 20, 2020	Still on market
Italy	May 20, 2020	Still on market
Liechtenstein	May 20, 2020	Still on market
Lithuania	May 20, 2020	Still on market
Luxembourg	May 20, 2020	Still on market
Netherlands	May 20, 2020	Still on market
Poland	May 20, 2020	Still on market
Portugal	May 20, 2020	Still on market
Romania	May 20, 2020	Still on market
Sweden	May 20, 2020	Still on market
Slovakia	May 20, 2020	Still on market
Türkiye	May 20, 2020	Still on market

Related searches

Class IIa medical devices in EUDAMED

Device identification

Trade name: Titanium cap
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 04099797010947
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. View in glossary →: 40997970004502000000000JQ
Reference / catalog number: J2259.6022
UDI issuing entities Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system. View in glossary →: GS1

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in Germany; available across 24 countries total.

Country	On market since	Until
GermanyPrimary placement	May 20, 2020	Still on market
Austria	May 20, 2020	Still on market
Belgium	May 20, 2020	Still on market
Bulgaria	May 20, 2020	Still on market
Czechia	May 20, 2020	Still on market
Denmark	May 20, 2020	Still on market
EL	May 20, 2020	Still on market
Spain	May 20, 2020	Still on market
Finland	May 20, 2020	Still on market
France	May 20, 2020	Still on market
Croatia	May 20, 2020	Still on market
Hungary	May 20, 2020	Still on market
Ireland	May 20, 2020	Still on market
Italy	May 20, 2020	Still on market
Liechtenstein	May 20, 2020	Still on market
Lithuania	May 20, 2020	Still on market
Luxembourg	May 20, 2020	Still on market
Netherlands	May 20, 2020	Still on market
Poland	May 20, 2020	Still on market
Portugal	May 20, 2020	Still on market
Romania	May 20, 2020	Still on market
Sweden	May 20, 2020	Still on market
Slovakia	May 20, 2020	Still on market
Türkiye	May 20, 2020	Still on market

Titanium cap

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Market distribution

Related searches

Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates

Certificates covering this device

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