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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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LaserBes — 1 UDI-DI variant, MDD (BES Srl)

MD Atlas
BES Srl

Data from EUDAMED, last updated May 30, 2026

LaserBes

B-LaserBes9H

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: BES Srl

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Device characteristics

Active device

Legacy certificates

Certificate number: IT281854
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: BUREAU VERITAS ITALIA S.P.A. (1370)
Validity: May 31, 2026

Identity & classification

Basic UDI-DI: B-LaserBes9H
Device name: LaserBes
Device model: LaserBes
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: May 4, 2026

Manufacturer & authorised representative

Manufacturer

Name: BES Srl
SRN: IT-MF-000034821
Country: Italy
Email: info@besitalia.it

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KQSCPQRETN38P70FJG9BN8AA

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

LaserBesD-LaserBes9H