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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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STERIKING® Hot Air Rolls — 6 UDI-DI variants, MDR (Wipak Oy)

MD Atlas
Wipak Oy

Data from EUDAMED, last updated May 23, 2026

STERIKING® Hot Air Rolls

6438263ST15012NW

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: Wipak Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 6438263ST15012NW
Device name: STERIKING® Hot Air Rolls
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 10, 2021

Manufacturer & authorised representative

Manufacturer

Name: Wipak Oy
SRN: FI-MF-000004496
Country: Finland
Email: info.fi.wn@wipak.com
Phone: +358 20 510 311

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01FPJ1VD6MQ6VP9CFY7BDRVKDV

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

HR3906438263922014
HR4206438263922045
HR4306438263922052
HR4006438263922021
HR4406438263922069
HR4106438263922038