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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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ME2200 — 1 UDI-DI variant, MDD (UNITEKNO S.R.L.)

MD Atlas
UNITEKNO S.R.L.

Data from EUDAMED, last updated May 31, 2026

ME2200

B-08021195000059

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: UNITEKNO S.R.L.

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Device characteristics

Active device

Legacy certificates

Certificate number: 1455/MDD
Type: refdata.legacy.mdd-certificate-type.v
Notified body: IMQ ISTITUTO ITALIANO DEL MARCHIO DI QUALITÀ S.P.A. (0051)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-08021195000059
Device name: —
Device model: ME2200
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Dec 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: UNITEKNO S.R.L.
SRN: IT-MF-000007398
Country: Italy
Email: info@unitekno.com
Phone: 0039 0742 24109

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KBCTNNAE2CQXA81C7M9ZEB62

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

ME220008021195000059