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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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Remo-Wax Oil — 4 UDI-DI variants, MDR (Orion Oyj)

MD Atlas
Orion Oyj

Data from EUDAMED, last updated May 23, 2026

Remo-Wax Oil

643210OIL001UB

4 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: Orion Oyj

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Device characteristics

No device characteristics flagged

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 643210OIL001UB
Device name: Remo-Wax Oil
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 21, 2025

Manufacturer & authorised representative

Manufacturer

Name: Orion Oyj
SRN: FI-MF-000001595
Country: Finland
Email: medicaldevice@orionpharma.com
Phone: +358104261

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JPS3W2ZVQTMC3SWTBR9385QB

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

16176206432100102164
14290406432100023919
14290506432100023971
14290806432100023926