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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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HP5500D — 2 UDI-DI variants, MDR (HERCO Wassertechnik GmbH)

MD Atlas
HERCO Wassertechnik GmbH

Data from EUDAMED, last updated May 23, 2026

HP5500D

42518152HY001AT

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: HERCO Wassertechnik GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42518152HY001AT
Device name: HP5500D
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: HERCO Wassertechnik GmbH
SRN: DE-MF-000007521
Country: Germany
Email: info@hercowater.com

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01FJEHNS7Y68ZM5ZPT8MF2WRGH

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

0046596304251815200017
0046590204251815200277