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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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pRELAX - Vasospasm Treatment Device — 1 UDI-DI variant, MDD

MD Atlas
femtos GmbH

Data from EUDAMED, last updated May 30, 2026

pRELAX - Vasospasm Treatment Device

B-04270000054105

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Manufacturer: femtos GmbH

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 523925 MR2
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: DQS Medizinprodukte GmbH (0297)
Validity: Dec 31, 2027

Identity & classification

Basic UDI-DI: B-04270000054105
Device name: pRELAX - Vasospasm Treatment Device
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Version date: Nov 12, 2021

Manufacturer & authorised representative

Manufacturer

Name: femtos GmbH
SRN: DE-MF-000005499
Country: Germany
Email: femtos.info@wallabyphenox.com
Phone: +49 234 970 50 320

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01FM9YF1P5ZM0TD5D3AWBCHGMB

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

pRELAX - Vasospasm Treatment Device04270000054105