EUDAMED last updated this device on Aug 4, 2026

Adequest Module

7332414VA0000132Q

On the marketClass IIa

Applicable legislation: —
Organization name: Vantive Health GmbH
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 →: 27332414254326
Reference / catalog number: 5CGM21

Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.

Adequest Module is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Vantive Health GmbH. Placed on the EU market in Northern Ireland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: Adequest Module
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 →: 27332414254326
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 →: 7332414VA0000132Q
Reference / catalog number: 5CGM21
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 →: GS1

Classification

Risk category: Class IIa
Applicable legislation: —
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://eu.sharesource.com/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)27332414254326

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z12090192PERITONEAL DIALYSIS INSTRUMENTS - MEDICAL DEVICE SOFTWARE

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

Caution
Consult instructions for use

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in XI; available across 17 countries total.

Country	On market since	Until
XIPrimary placement	—	Still on market
Austria	—	Still on market
Belgium	—	Still on market
Germany	—	Still on market
Denmark	—	Still on market
EL	—	Still on market
Spain	—	Still on market
France	—	Still on market
Ireland	—	Still on market
Italy	—	Still on market
Luxembourg	—	Still on market
Netherlands	—	Still on market
Norway	—	Still on market
Poland	—	Still on market
Sweden	—	Still on market
Slovenia	—	Still on market
Türkiye	—	Still on market

Related searches

Class IIa medical devices in EUDAMED

Device identification

Trade name: Adequest Module
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 →: 27332414254326
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 →: 7332414VA0000132Q
Reference / catalog number: 5CGM21
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 →: GS1

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Certificates

Certificate health across this manufacturer's portfolio.

G15 123153 0024Issued
Quality management system: TÜV SÜD Product Service GmbH (0123)Expiry: Jan 11, 2028
G70 123153 0023Issued
Technical documentation: TÜV SÜD Product Service GmbH (0123)Expiry: Jan 9, 2028
G12 123153 0017Issued
Quality management system: TÜV SÜD Product Service GmbH (0123)Expiry: Jan 30, 2030
G12 123153 0018Issued
Quality management system: TÜV SÜD Product Service GmbH (0123)Expiry: Dec 18, 2029

Market distribution

Primary placement in XI; available across 17 countries total.

Country	On market since	Until
XIPrimary placement	—	Still on market
Austria	—	Still on market
Belgium	—	Still on market
Germany	—	Still on market
Denmark	—	Still on market
EL	—	Still on market
Spain	—	Still on market
France	—	Still on market
Ireland	—	Still on market
Italy	—	Still on market
Luxembourg	—	Still on market
Netherlands	—	Still on market
Norway	—	Still on market
Poland	—	Still on market
Sweden	—	Still on market
Slovenia	—	Still on market
Türkiye	—	Still on market

Adequest Module

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Market distribution

Related searches

Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates covering this device

Related devices

Certificates