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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

HVCF30 — Class I MDR by MUTSUMI DENTAL SRL

MD Atlas
MUTSUMI DENTAL SRL

EUDAMED last updated this device on May 26, 2022

HVCF30

5944759013MASADEAMBALATET

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MUTSUMI DENTAL SRL
UDI-DI code: 05944759013957
Reference / catalog number: HVCF30

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Manufacturer information

Organization name: MUTSUMI DENTAL SRL
SRN: RO-MF-000024238
Manufacturer status: Active

Critical warnings

5 warnings recorded — scroll inside the panel to see all entries.

CW044
EUDAMED did not publish a description for this code.
CW158
EUDAMED did not publish a description for this code.
CW321
EUDAMED did not publish a description for this code.
CW101
EUDAMED did not publish a description for this code.
CW102
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Romania; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 05944759013957
Basic UDI-DI: 5944759013MASADEAMBALATET
Reference / catalog number: HVCF30
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: 1
Additional product description: Masa de ambalat fosfatica pentru machete din ceara, rasini printabile 3D, pattern resin.
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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Related devices

This device is not currently linked to any other device.

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.