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EUDAMED last updated this device on Apr 11, 2023
5604425SSPFFFJ 70L 1PD (32*32*70) is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by PROHS Equipamento Hospitalar e Serviços Associados S.A.. Placed on the EU market in Portugal. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
05604425000000FJ 70L 1PD (32*32*70)(01)05604425000000
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12011304AUTOCLAVES WITH A CHAMBER LARGER THAN OR EQUAL TO 1 STANDARD STERILISATION UNITPT-MF-000002798ES23/00000293The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Portugal; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| PortugalPrimary placement | — | Still on market |
| Bulgaria | — | Still on market |
| France | — | Still on market |
| Poland | — | Still on market |
| Romania | — | Still on market |
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →B-05604425001106On the marketPROHS HORIZONTAL STEAM STERILIZERB-05604425001212On the marketFJ 100L 1PD (32*32*100)5604425SSPFFOn the marketFJ 145L 1PD (40*40*90)5604425SSPFFOn the marketFJ 930L 1PD (70*70*190)5604425SSPFFOn the marketFJ 175L 2PD (50*50*70)5604425SSPFFOn the marketCertificate health across this manufacturer's portfolio.
ES23/00000293AmendedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
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