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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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PROHS Horizontal Steam Sterilizer — 1 UDI-DI variant, MDD

MD Atlas
PROHS Equipamento Hospitalar e Serviços Associados S.A.

Data from EUDAMED, last updated May 30, 2026

PROHS Horizontal Steam Sterilizer

B-05604425000000

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: PROHS Equipamento Hospitalar e Serviços Associados S.A.

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Device characteristics

Active device

Legacy certificates

Certificate number: ES19/86765.00
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: SGS Belgium NV (1639)
Validity: Feb 20, 2023

Identity & classification

Basic UDI-DI: B-05604425000000
Device name: PROHS Horizontal Steam Sterilizer
Device model: FJ 70L 1PD (32*32*70)
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Jan 7, 2022

Manufacturer & authorised representative

Manufacturer

Name: PROHS Equipamento Hospitalar e Serviços Associados S.A.
SRN: PT-MF-000002798
Country: Portugal
Email: prohs@prohs.pt
Phone: +351229059170

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01FHAFTG0M94TE0Z84D3X9R5DW

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

Horizontal Steam Sterilizer05604425000000