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

MD Atlas
Disentis AB

Data from EUDAMED, last updated May 31, 2026

008 Waye Readers

7350145WR0008ME

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: 7350145WR0008ME
Device name: 008 Waye Readers
Device model: WR0008
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 17, 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

basicUdiUlid01KKXNRK6NNVHBR29HRCY95RZA

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

008 Waye Readers Black / Readers 1007350145359567
008 Waye Readers Black / Readers 1507350145359574
008 Waye Readers Black / Readers 2007350145359581
008 Waye Readers Black / Readers 2507350145359598
008 Waye Readers Black / Readers 3007350145359604
008 Waye Readers Black / Readers 3507350145359611