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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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Relegs Device Product - BOX -Re-launch — 1 UDI-DI variant, MDD

MD Atlas
RELEGS BV

Data from EUDAMED, last updated May 30, 2026

Relegs Device Product - BOX -Re-launch

B-08719327508909

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: RELEGS BV

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Device characteristics

Active device

Legacy certificates

Certificate number: 19M00096CRT02
Type: refdata.legacy.mdd-certificate-type.iv
Notified body: Kiwa Assurance B.V. (1912)
Validity: May 27, 2024

Identity & classification

Basic UDI-DI: B-08719327508909
Device name: Relegs Device Product - BOX -Re-launch
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Jan 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: RELEGS BV
SRN: NL-MF-000005880
Country: Netherlands
Email: support@relegs.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01JH0RP0DK8347WBRWWYFE79EG

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

Relegs08719327508909