EUDAMED last updated this device on Jun 24, 2026

Scan Body for internal hex, Peek+Ti Base

729010881ScanAbut1ZD

On the marketClass I

Applicable legislation: —
Organization name: NORIS MEDICAL Ltd
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 →: 07290108817171
Reference / catalog number: NM-C9013

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.

Scan Body for internal hex, Peek+Ti Base is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by NORIS MEDICAL Ltd. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: Scan Body for internal hex, Peek+Ti Base
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 →: 07290108817171
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 →: 729010881ScanAbut1ZD
Reference / catalog number: NM-C9013
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 I
Applicable legislation: —
Status: On the market

Device details

Quantity: 1
Additional product description: The Scanning abutments are Non-Invasive devices intended to represent the position and orientation of the respective dental implant, analog, or abutment in scanning procedures.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 13 MU50

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)07290108817171

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.

Q010207DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY

Critical warnings

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

Do not use if package is damaged
Consult instructions for use

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	—	Still on market

Scan Body for internal hex, Peek+Ti Base

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

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Market distribution

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Manufacturer information

Certificates

Certificates covering this device

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