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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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RefluxStop Deployment Tool — 1 UDI-DI variant, MDR

MD Atlas
Implantica CE Reflux Ltd.

Data from EUDAMED, last updated May 30, 2026

RefluxStop Deployment Tool

5350646RS300SX

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Implantica CE Reflux Ltd.

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 5350646RS300SX
Device name: RefluxStop Deployment Tool
Device model: RS-300
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: Implantica CE Reflux Ltd.
SRN: MT-MF-000002866
Country: Malta
Email: Melanie.Houselog@implantica.com
Phone: +41 41 539 19 00

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KS7XP10Y3N5CPC3PH7XZ3YW0

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

RS-30005350646999912