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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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Metode neseolje m/vitA — 5 UDI-DI variants, MDR (Pharmia Oy)

MD Atlas
Pharmia Oy

Data from EUDAMED, last updated May 23, 2026

Metode neseolje m/vitA

641795210002CD

5 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: Pharmia Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 641795210002CD
Device name: Metode neseolje m/vitA
Device model: 10 ml
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 5, 2023

Manufacturer & authorised representative

Manufacturer

Name: Pharmia Oy
SRN: FI-MF-000001469
Country: Finland
Email: info@pharmia.fi

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01HGWMF56FWEX5FEKYEEC7D6JE

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

LPXG0106417952244163
LPXG0206417952244170
LORN78 [FI] / LORN78.2 [PL] 06417952243876
LORN9706417952243890
LORN96 [FI] / LORN96.2 [PL]06417952243883