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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

R2620RA-100 — Class IIa MDR by Edenta Etablissement

MD Atlas
Edenta Etablissement

EUDAMED last updated this device on Nov 10, 2022

R2620RA-100

++E31216412DU

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Edenta Etablissement
UDI-DI code: E312R2620RA1001
Reference / catalog number: R2620RA-100

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View device family (Basic UDI)

Manufacturer information

Organization name: Edenta Etablissement
SRN: LI-MF-000011937
Manufacturer status: Active

Related devices

0055FG-12++E31216412DUOn the market 0053FG-12++E31216412DUOn the market 0055FG-100++E31216412DUOn the market 0053FG-100++E31216412DUOn the market 0153FG-12++E31216412DUOn the market

Certificates

Certificate health across this manufacturer's portfolio.

1000183128Issued
Quality management systemNotified body: 0297Expiry: Mar 26, 2030

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Liechtenstein; available across 1 country total.

Country	On market since	Until
LiechtensteinPrimary placement	Dec 1, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: E312R2620RA1001
Basic UDI-DI: ++E31216412DU
Reference / catalog number: R2620RA-100
Issuing entity: HIBCC

Classification

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

Device details

Quantity: 100
Additional product description: —
Additional information URL: https://www.edenta.com/
Clinical sizes: 6 MU50

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

E312R2620RA1001

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

EMDN nomenclature code(s)

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

Q01010403DENTAL ABRASIVE AND POLISHING MATERIALS

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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