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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

CALXYL® X-RAY VISIBLE — Class IIa MDD by OCO-Präparate…

MD Atlas
OCO-Präparate Herstellung und Vertrieb von pharmazeutischen Produkten GmbH

EUDAMED last updated this device on Oct 7, 2022

CALXYL® X-RAY VISIBLE

B-04260741310059

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: OCO-Präparate Herstellung und Vertrieb von pharmazeutischen Produkten GmbH
UDI-DI code: 04260741310059
Reference / catalog number: 11400200

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Manufacturer information

Organization name: OCO-Präparate Herstellung und Vertrieb von pharmazeutischen Produkten GmbH
SRN: DE-MF-000012362
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Feb 1, 1960	Still on market

Device identification

Trade name: CALXYL® X-RAY VISIBLE
UDI-DI code: 04260741310059
Basic UDI-DI: B-04260741310059
Reference / catalog number: 11400200
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Calcium hydroxide Suspension in paste form for care free dentin close to pulp; caries profunda treatment; direct and indirect pulp capping; pulpotomy; root canal treatment
Additional information URL: https://www.oco-praeparate.de/en/p/calxyl/
Clinical sizes: 20 g

EMDN nomenclature code(s)

Q01010201ROOT CANAL FILLING DENTAL PASTES

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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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.