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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

41907 — Class I MDR by Polydentia SA

MD Atlas
Polydentia SA

EUDAMED last updated this device on Jul 7, 2025

41907

++E299PDMATRICES74

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Polydentia SA
UDI-DI code: +E299419070
Reference / catalog number: 41907

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Manufacturer information

Organization name: Polydentia SA
SRN: CH-MF-000008779
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

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

CW011
Use only with rubber dam

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: +E299419070
Basic UDI-DI: ++E299PDMATRICES74
Reference / catalog number: 41907
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: 50
Additional product description: molar with extension 0.04mm
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: Thickness — 0.04 MU50
8.4 MU50

EMDN nomenclature code(s)

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification