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Organization name
UDI-DI code
Reference / catalog number

VILLACRYL H RADPID FN V4 24g powder — Class I MDR

MD Atlas
EVERALL7 SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ

EUDAMED last updated this device on May 12, 2026

VILLACRYL H RADPID FN V4 24g powder

590160212DBQ3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: EVERALL7 SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ
UDI-DI code: 05901602125298
Reference / catalog number: V260V4P02

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Manufacturer information

Organization name: EVERALL7 SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ
SRN: PL-MF-000018646
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

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

CW999
Do not use the products by people diagnosed with a lack of resistance to allergenic factors, including the ingredients of the product. In such situations, use a different material suitable for the patient
CW999
Do not use the product by pregnant women and nursing mothers in the group of dental technicians
CW082
EUDAMED did not publish a description for this code.
CW083
Contains Benzoyl Peroxide
CW159
EUDAMED did not publish a description for this code.
CW162
EUDAMED did not publish a description for this code.
CW167
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement		Still on market

Device identification

Trade name: VILLACRYL H RADPID FN V4 24g powder
UDI-DI code: 05901602125298
Basic UDI-DI: 590160212DBQ3
Reference / catalog number: V260V4P02
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: heat-curing acrylic resin for removable dentures
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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