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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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DDS50 FLUID — 1 UDI-DI variant, MDD (Mondial Srl)

MD Atlas
Mondial Srl

Data from EUDAMED, last updated May 30, 2026

DDS50 FLUID

B-FM126266

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: Mondial Srl

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 25296/1
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: CERTIQUALITY S.r.l. (0546)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-FM126266
Device name: DDS50 FLUID
Device model: FT21
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Jan 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: Mondial Srl
SRN: IT-MF-000022978
Country: Italy
Email: info@mondialprod.it
Phone: +39 049 768712

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KFN1S4NGD0245AS1NJAZ4N92

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

FM1262D-FM126266