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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

IPS InLine Sy Powder Opaquer 18g C2 — Class IIa MDR

MD Atlas
Ivoclar Vivadent AG

EUDAMED last updated this device on May 18, 2026

IPS InLine Sy Powder Opaquer 18g C2

76152082ACERA011ET

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Ivoclar Vivadent AG
UDI-DI code: 07615208350920
Reference / catalog number: 649181

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View device family (Basic UDI)

Manufacturer information

Organization name: Ivoclar Vivadent AG
SRN: LI-MF-000000522
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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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: IPS InLine Sy Powder Opaquer 18g C2
UDI-DI code: 07615208350920
Basic UDI-DI: 76152082ACERA011ET
Reference / catalog number: 649181
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: IPS InLine Sy Powder Opaquer 18g C2
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

EMDN nomenclature code(s)

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

Q010699MATERIALS FOR THE PREPARATION OF CUSTOM-MADE DENTAL 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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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.