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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 — 1 UDI-DI variant, MDD (Implantica CE Reflux Ltd.)

MD Atlas
Implantica CE Reflux Ltd.

Data from EUDAMED, last updated May 30, 2026

RefluxStop

B-05350646999905

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: Implantica CE Reflux Ltd.

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Device characteristics

Implantable

Clinical investigations

Registered: No

Legacy certificates

Certificate number: CE660601
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: BSI Group The Netherlands B.V. (2797)
Validity: Aug 7, 2023

Identity & classification

Basic UDI-DI: B-05350646999905
Device name: RefluxStop
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Oct 3, 2022

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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Applied filters

basicUdiUlid01GEENWW48YJAJ7SM0N3SNPWGQ

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-A105350646999905