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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 Korotustyynyt — 6 UDI-DI variants, MDR

MD Atlas
Carpenter Engineered Foams Oy

Data from EUDAMED, last updated May 23, 2026

Fysicon Korotustyynyt

6438142FFC5BRB

6 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: 6438142FFC5BRB
Device name: Fysicon Korotustyynyt
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 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

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HYTPN1SK2BTDDST5ZB9W0SZC

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

350100691306438142069137
350101008106438142100816
350101008206438142100823
350101008306438142100830
350101008506438142100854
350101008406438142100847