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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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D.B.M. AQUAFLUSH, D.B.M. AQUAGLY,… — 3 UDI-DI variants, MDR (DBM SRL)

MD Atlas
DBM SRL

Data from EUDAMED, last updated May 31, 2026

D.B.M. AQUAFLUSH, D.B.M. AQUAGLY, D.B.M. AQUAGLY-NS

805620966DBMWATERFLUSHDB

3 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: DBM SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805620966DBMWATERFLUSHDB
Device name: D.B.M. AQUAFLUSH, D.B.M. AQUAGLY, D.B.M. AQUAGLY-NS
Device model: D.B.M. WATERFLUSH
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 25, 2025

Manufacturer & authorised representative

Manufacturer

Name: DBM SRL
SRN: IT-MF-000017565
Country: Italy
Email: info.dbm@numantec.eu
Phone: 0039 342771613

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KAWZ2AYAZ11WRC85EBR2HYE2

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

PAG01NB1TG38056209661781
PCG01MB1TG38056209661644
PCG08NB1TG38056209661989