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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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F2 — 1 UDI-DI variant, MDD

MD Atlas
I.P.S. INTERNATIONAL PRODUCTS e SERVICES Srl

Data from EUDAMED, last updated May 30, 2026

F2

B-08008687000087

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: I.P.S. INTERNATIONAL PRODUCTS e SERVICES Srl

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Device characteristics

Measuring function

Legacy certificates

Certificate number: 1271/MDD
Type: refdata.legacy.mdd-certificate-type.vi
Notified body: IMQ ISTITUTO ITALIANO DEL MARCHIO DI QUALITÀ S.P.A. (0051)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-08008687000087
Device name: F2
Device model: F2
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: Mar 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: I.P.S. INTERNATIONAL PRODUCTS e SERVICES Srl
SRN: IT-MF-000029091
Country: Italy
Email: info@ips-srl.it
Phone: +39025279641

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01JPJ7G83P13MPP9G3X1Q0FDJ5

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

F208008687000087