- Organization name
- UDI-DI code
- Reference / catalog number
AR-MF-000047833VERISURE™ Steam Type 5 Ink Integrator is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Terragene S.A.. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Apr 30, 2026
779816467CI5LPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)07798375772952
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
2 warnings recorded — scroll inside the panel to see all entries.
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.
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.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Netherlands; available across 14 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | — | Still on market |
| Austria | — | Still on market |
| Belgium | — | Still on market |
| Germany | — | Still on market |
| Denmark | — | Still on market |
| Spain | — | Still on market |
| Finland | — | Still on market |
| France | — | Still on market |
| Croatia | — | Still on market |
| Italy | — | Still on market |
| Norway | — | Still on market |
| Poland | — | Still on market |
| Portugal | — | Still on market |
| Sweden | — | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
07798375772952Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
779816467CI5L73156UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
1 packaging level registered — each level carries its own UDI-DI.
07798375772952× 200 unitsBase unit07798375772969× 2 unitsEuropean Medical Device Nomenclature — the EU product classification assigned to this device.
S9080DEVICES FOR STERILISATION (EXCLUDING CAT. D - Z) - ACCESSORIESNo certificate specifically references this device's Basic UDI-DI.
779816467CI5LOn the marketVERISURE™ EO Type 4 Multi-Variable Chemical Indicator Strip779816467CI5LOn the marketVERISURE™ Steam Type 4 Multi-Variable Chemical Indicator779816467CI5LOn the marketVERISURE™ Steam Type 5 Migrating Integrator Process Challenge Device779816467CI5LOn the marketVERISURE™ Steam Type 5 Migrating Integrator w/ Extender779816467CI5LOn the marketVERISURE™ Ultrasonic Cavitation Test779816467CI5LOn the marketNo certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.