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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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Wake Up Drying Tablets — 2 UDI-DI variants, MDR

MD Atlas
Wake Up International B.V.

Data from EUDAMED, last updated May 30, 2026

Wake Up Drying Tablets

8720791017613389654974LB

2 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: Wake Up International B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8720791017613389654974LB
Device name: Wake Up Drying Tablets
Device model: Wake Up Drying Tablets
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 16, 2024

Manufacturer & authorised representative

Manufacturer

Name: Wake Up International B.V.
SRN: NL-MF-000023964
Country: Netherlands
Email: info@wake.nl
Phone: +31 030 697 32 40

Variants by status

UDI-DI variants

2 UDI-DI variants

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basicUdiUlid01HY0Q8320N1GJXF4NW5095T08

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

40900707007613389394818
40900778307613389654974