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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

7153 — Class I MDR by CB Dental Reg. GmbH

MD Atlas
CB Dental Reg. GmbH

EUDAMED last updated this device on May 11, 2026

7153

++D92504881000000005K

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CB Dental Reg. GmbH
UDI-DI code: +D92571531
Reference / catalog number: 7153

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Manufacturer information

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

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9796086++D925056900110389896On the market 9796087++D925056900110389896On the market 9790506++D92506370011038985LOn the market 9888888++D9250107001103897UROn the market 8653++D92509370600000008FOn 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.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jan 1, 2020	Still on market

Device identification

Trade name: not provided
UDI-DI code: +D92571531
Basic UDI-DI: ++D92504881000000005K
Reference / catalog number: 7153
Issuing entity: HIBCC

Classification

Risk category: Class I
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: 1000 MU24

EMDN nomenclature code(s)

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

UDI-PI traceability

Batch number
Expiration date
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Software identification