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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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016 Waye Readers — 6 UDI-DI variants, MDR (Disentis AB)

MD Atlas
Disentis AB

Data from EUDAMED, last updated May 31, 2026

016 Waye Readers

73402289WR0016EK

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: Disentis AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73402289WR0016EK
Device name: 016 Waye Readers
Device model: WR0016R
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Disentis AB
SRN: SE-MF-000050466
Country: Sweden
Email: Order@disentis.se
Phone: 031-16 96 00

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KR1D107P32CWR0WX318HGEQZ

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

016 Waye Readers transparent clear +1,007340228909574
016 Waye Readers transparent clear +1,507340228909581
016 Waye Readers transparent clear +2,007340228909598
016 Waye Readers transparent clear +2,507340228909604
016 Waye Readers transparent clear +3,007340228909611
016 Waye Readers transparent clear +3,507340228909628