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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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BM-33T — 1 UDI-DI variant, MDD (S.I.D.EM. S.p.A.)

MD Atlas
S.I.D.EM. S.p.A.

Data from EUDAMED, last updated May 30, 2026

BM-33T

B-08050624190177

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: S.I.D.EM. S.p.A.

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Device characteristics

Active device

Legacy certificates

Certificate number: G10765960008
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: TÜV SÜD Product Service GmbH (0123)
Validity: May 26, 2024

Identity & classification

Basic UDI-DI: B-08050624190177
Device name: BM-33T
Device model: Multi-shot
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Apr 18, 2024

Manufacturer & authorised representative

Manufacturer

Name: S.I.D.EM. S.p.A.
SRN: IT-MF-000029977
Country: Italy
Email: lorenzo.om.banfi@sidemspa.it
Phone: +393518009161

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01HVR8DJJ5XVHNXMN74638RKXD

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

TEE Care System08050624190177