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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

9001013 — Class IIa MDR by CB Dental Reg. GmbH

MD Atlas
CB Dental Reg. GmbH

EUDAMED last updated this device on May 8, 2026

9001013

++D92506370011038975J

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CB Dental Reg. GmbH
UDI-DI code: +D92590010131
Reference / catalog number: 9001013

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Manufacturer information

Organization name: CB Dental Reg. GmbH
SRN: DE-MF-000005407
Manufacturer status: Active

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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.

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	Mar 7, 1996	Still on market

Device identification

Trade name: not provided
UDI-DI code: +D92590010131
Basic UDI-DI: ++D92506370011038975J
Reference / catalog number: 9001013
Issuing entity: HIBCC

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: 2 MU03

EMDN nomenclature code(s)

Q0101010299TEMPORARY AND PERMANENT DENTAL RESTORATION CEMENTS - 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

UDI-PI traceability

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Expiration date
Manufacturing date
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Software identification