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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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Fysicon MiniMAX patja — 3 UDI-DI variants, MDR

MD Atlas
Carpenter Engineered Foams Oy

Data from EUDAMED, last updated May 23, 2026

Fysicon MiniMAX patja

6438142FFC2AQY

3 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Carpenter Engineered Foams Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 6438142FFC2AQY
Device name: Fysicon MiniMAX patja
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 11, 2024

Manufacturer & authorised representative

Manufacturer

Name: Carpenter Engineered Foams Oy
SRN: FI-MF-000040986
Country: Finland
Email: henna.ahonen@carpenter.com
Phone: +358405537843

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J03RGFMQD1QSZBF6PCW1YXAB

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

350100946606438142094665
350100754306438142075435
350100766106438142076616