Organization name

ALTATEC GmbH

SRN

DE-MF-000006230

Manufacturer status

Active

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

Primary placement in Germany; available across 24 countries total.

Trade name

CONELOG® Impression post

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.

04099797010138

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.

40997970006016000000000L4

Reference / catalog number

CA2137.4340

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.

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.

Class I

Applicable legislation

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

Status

On the market

Quantity

1

Additional product description

CONELOG® Impression post for closed tray, ML, Ø 4.3 mm, GH 4.0 mm

Additional information URL

https://ifu.camlog.com/

Clinical sizes

• 4.3 MU50
• Gingival height — 4 MU50

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification

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

• P01020180DENTAL IMPLANTS - ACCESSORIES

• Class I medical devices in EUDAMED

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

Certificate health across this manufacturer's portfolio.