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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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Farmaka FMS Protector Spray — 1 UDI-DI variant, MDD (Farmaka srl)

MD Atlas
Farmaka srl

Data from EUDAMED, last updated May 30, 2026

Farmaka FMS Protector Spray

B-IT-MF-000024545BH

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: Farmaka srl

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 22303/1
Type: refdata.legacy.mdd-certificate-type.v
Notified body: CERTIQUALITY S.r.l. (0546)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-IT-MF-000024545BH
Device name: Farmaka FMS Protector Spray
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Mar 28, 2023

Manufacturer & authorised representative

Manufacturer

Name: Farmaka srl
SRN: IT-MF-000024545
Country: Italy
Email: qa.ra@farmaka.com
Phone: +39 02 33497026

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01GWM4HF6HC3YBHJCB8GCH4V9J

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

E418 (Australia); E403 (HK)D-IT-MF-000024545BH