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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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D-Reamer — 31 UDI-DI variants, MDR (QuantièmePlus SA)

MD Atlas
QuantièmePlus SA

Data from EUDAMED, last updated May 23, 2026

D-Reamer

764016863REUTJS

31 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: QuantièmePlus SA

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 764016863REUTJS
Device name: D-Reamer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 22, 2022

Manufacturer & authorised representative

Manufacturer

Name: QuantièmePlus SA
SRN: CH-MF-000011186
Country: Switzerland
Email: frederic.mani@quantiemeplus.com

Authorised representative

Name: LAPE Médical
SRN: FR-AR-000007694
Country: France
Phone: +33 4899584

Variants by status

UDI-DI variants

31 UDI-DI variants

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Applied filters

basicUdiUlid01GMX2S2EQZ0FW9PTR8QTRS1BQ

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

No registered UDI-DI variants for this device family.