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

MD Atlas
Disentis AB

Data from EUDAMED, last updated May 30, 2026

010 Waye Readers

7350145WR0010LZ

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: 7350145WR0010LZ
Device name: 010 Waye Readers
Device model: WR0010
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 19, 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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Applied filters

basicUdiUlid01KM3Q5NQNSH88P0K0H21CP4A7

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

010 Waye Readers Milky Purple / Readers 1007350145359680
010 Waye Readers Milky Purple / Readers 1507350145359697
010 Waye Readers Milky Purple / Readers 2007350145359703
010 Waye Readers Milky Purple / Readers 2507350145359710
010 Waye Readers Milky Purple / Readers 3007350145359727
010 Waye Readers Milky Purple / Readers 3507350145359734