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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

PROB40001AR — Class I MDR by PERIDENT DENTAL…

MD Atlas
PERIDENT DENTAL PRODUCTS s.r.l.

EUDAMED last updated this device on Apr 20, 2026

PROB40001AR

805697705048451R02XT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PERIDENT DENTAL PRODUCTS s.r.l.
UDI-DI code: 08056977050885
Reference / catalog number: PROB40001AR

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View device family (Basic UDI)

Manufacturer information

Organization name: PERIDENT DENTAL PRODUCTS s.r.l.
SRN: IT-MF-000044166
Manufacturer status: Active

Related devices

PROB40001BI805697705048451R02XTOn the market PROB40001BLU805697705048451R02XTOn the market PROB40001VIO805697705048451R02XTOn the market PROB40001GIAL805697705048451R02XTOn the market PROB40001ROSA805697705048451R02XTOn 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

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08056977050885
Basic UDI-DI: 805697705048451R02XT
Reference / catalog number: PROB40001AR
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: —
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

UDI-DI DataMatrix

Encoded

(01)08056977050885

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Q01010401PAPER AND GUTTA-PERCHA TIPS, MATRICES AND WEDGES FOR DENTISTRY

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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