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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

645003 — Class I MDR by Dentalia Dentálgyártmány…

MD Atlas
Dentalia Dentálgyártmány Kft.

EUDAMED last updated this device on Jul 29, 2022

645003

5999861682dentalbibsUE

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Dentalia Dentálgyártmány Kft.
UDI-DI code: 05999861682225
Reference / catalog number: 645003

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Manufacturer information

Organization name: Dentalia Dentálgyártmány Kft.
SRN: HU-MF-000008310
Manufacturer status: Active

Critical warnings

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

CW009
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Hungary; available across 1 country total.

Placed on the market in Hungary; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 05999861682225
Basic UDI-DI: 5999861682dentalbibsUE
Reference / catalog number: 645003
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 200
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 56 MU10
77 MU10

EMDN nomenclature code(s)

T0306PATIENT PROTECTION DEVICES DURING CLINICAL PROCEDURES

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.