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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

211710Pow. — Class IIa MDR by Estetic Ceram AG

MD Atlas
Estetic Ceram AG

EUDAMED last updated this device on May 12, 2026

211710Pow.

7630503100007H

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Estetic Ceram AG
UDI-DI code: 07630503103828
Reference / catalog number: 211710Pow.

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View device family (Basic UDI)

Manufacturer information

Organization name: Estetic Ceram AG
SRN: LI-MF-000001476
Manufacturer status: Active

Related devices

8.08.06.01477630503100007HOn the market 8.08.06.01507630503100007HOn the market 8.08.06.01497630503100007HOn the market 8.08.06.01487630503100007HOn the market 8.08.06.01037630503100007HOn the market

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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Liechtenstein; available across 1 country total.

Country	On market since	Until
LiechtensteinPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 07630503103828
Basic UDI-DI: 7630503100007H
Reference / catalog number: 211710Pow.
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: —
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)07630503103828

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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.

Q010199CONSERVATIVE DENTISTRY AND ENDODONTICS DEVICES - OTHER

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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