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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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CUFFIA CM. 90 C/ELASTICO — 1 UDI-DI variant, MDD (Delta Med SPA)

MD Atlas
Delta Med SPA

Data from EUDAMED, last updated May 30, 2026

CUFFIA CM. 90 C/ELASTICO

B-08032248850019

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: Delta Med SPA

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: G2S 026056 0029
Type: refdata.legacy.mdd-certificate-type.v
Notified body: TÜV SÜD Product Service GmbH (0123)
Validity: Nov 14, 2023

Identity & classification

Basic UDI-DI: B-08032248850019
Device name: CUFFIA CM. 90 C/ELASTICO
Device model: CUFFIA CM. 90 C/ELASTICO
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: Sep 5, 2024

Manufacturer & authorised representative

Manufacturer

Name: Delta Med SPA
SRN: IT-MF-000027962
Country: Italy
Email: info@numantec.eu

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01J716H6XKVHG8240X9J1YJCDN

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

12.A3121.0008032248850019