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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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Cutanplast — 1 UDI-DI variant, MDD (Mascia Brunelli S.p.A.)

MD Atlas
Mascia Brunelli S.p.A.

Data from EUDAMED, last updated May 30, 2026

Cutanplast

B-08033737980002

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Manufacturer: Mascia Brunelli S.p.A.

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Device characteristics

ImplantableAnimal tissues / cells

Legacy certificates

Certificate number: D1016000036
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: mdc medical device certification GmbH (0483)
Validity: Aug 29, 2023

Certificate number: D1016000045
Type: refdata.legacy.mdd-certificate-type.ii-4
Notified body: mdc medical device certification GmbH (0483)
Validity: Nov 6, 2023

Identity & classification

Basic UDI-DI: B-08033737980002
Device name: Cutanplast
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Version date: Oct 12, 2021

Manufacturer & authorised representative

Manufacturer

Name: Mascia Brunelli S.p.A.
SRN: IT-MF-000009572
Country: Italy
Email: mktg@masciabrunelli.it
Phone: +39 02.252091

Variants by status

UDI-DI variants

1 UDI-DI variant

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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

0517050208033737980002