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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® Paper Bags — 18 UDI-DI variants, MDR (Wipak Oy)

MD Atlas
Wipak Oy

Data from EUDAMED, last updated May 23, 2026

STERIKING® Paper Bags

6438263ST15011NU

18 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: 6438263ST15011NU
Device name: STERIKING® Paper Bags
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

18 UDI-DI variants

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Applied filters

basicUdiUlid01FPJAXMA4BYZWXFP6QXX00FY2

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

PB906438263924094
PB406438263924049
PB506438263924056
PB706438263924070
PB106438263924018
PB606438263924063
PB501 FLAT06438263665959
PB206438263924025
PB60106438263665911
PB306438263924032
PB806438263924087
PB90106438263665904
PB1006438263924100
PB1206438263924117
PB10106438263665935
PB006438263665942
PB0 FLAT06438263665966
PB20106438263665928