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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

3 Expander 6mm laser mark — Class IIa MDR by MOZO GRAU SA

MD Atlas
MOZO GRAU SA

EUDAMED last updated this device on May 25, 2026

3 Expander 6mm laser mark

84354826EXPANDERDK

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MOZO GRAU SA
UDI-DI code: 08435482639431
Reference / catalog number: 132030463

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View device family (Basic UDI)

Manufacturer information

Organization name: MOZO GRAU SA
SRN: ES-MF-000009479
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Spain; available across 3 countries total.

Country	On market since	Until
SpainPrimary placement		Still on market
Poland		Still on market
Romania		Still on market

Device identification

Trade name: 3 Expander 6mm laser mark
UDI-DI code: 08435482639431
Basic UDI-DI: 84354826EXPANDERDK
Reference / catalog number: 132030463
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: TICARE DENTAL EXPANDERS OF TICARE DENTAL IMPLANT SYSTEM
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08435482639431

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UDI-PI DataMatrix

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

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EMDN nomenclature code(s)

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

L159007ODONTOSTOMATOLOGY BURS, REUSABLE

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.