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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

RM20 — Class IIa MDR by QuantièmePlus SA

MD Atlas
QuantièmePlus SA

EUDAMED last updated this device on Oct 2, 2025

RM20

764016863REUTJS

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: QuantièmePlus SA
UDI-DI code: 07640168630201
Reference / catalog number: RM20

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Manufacturer information

Organization name: QuantièmePlus SA
SRN: CH-MF-000011186
Manufacturer status: Active

Related devices

RM36764016863REUTJSOn the market RM32764016863REUTJSOn the market RM37764016863REUTJSOn the market RM34764016863REUTJSOn the market RM31764016863REUTJSOn the market

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Oct 7, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: 07640168630201
Basic UDI-DI: 764016863REUTJS
Reference / catalog number: RM20
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: The Medical Device D-Reamer consists in a range of non-sterile reusable reamers, used for the establishment of a hip cup during a THA. RM20 = T68
Additional information URL: https://ifu.quantiemeplus.com/
Clinical sizes: 68 MU50

EMDN nomenclature code(s)

L091102ORTHOPAEDIC PROSTHESES REAMERS AND BURS, REUSABLE

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

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.