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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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BUG — 40 UDI-DI variants, MDR (ORMESA S.r.l.)

MD Atlas
ORMESA S.r.l.

Data from EUDAMED, last updated May 30, 2026

BUG

805571570BUGL9

40 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: ORMESA S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805571570BUGL9
Device name: BUG
Device model: BUG
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 31, 2025

Manufacturer & authorised representative

Manufacturer

Name: ORMESA S.r.l.
SRN: IT-MF-000034824
Country: Italy
Email: info@ormesa.com
Phone: 074222927

Variants by status

UDI-DI variants

40 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K1FKSKSRR5WBQHA3G4J6D8RF

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

4708055715703304
4708055715703311
4708055715703489
4708055715703496
4708055715703465
4708055715703335
4708055715703472
4708055715703168
4708055715703175
4708055715703144
4708055715703151
4708055715703007
4708055715703014
4708055715702987
4708055715702994

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