EUDAMED last updated this device on Jun 5, 2026

ENTONNOIR

366710600012ENTONNOIRPP

On the marketClass I

Applicable legislation: —
Organization name: AGENCINOX SAS
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 →: 03667106000579
Reference / catalog number: ENTONNOIR

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.

ENTONNOIR is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by AGENCINOX SAS. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: not provided
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 →: 03667106000579
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 →: 366710600012ENTONNOIRPP
Reference / catalog number: ENTONNOIR
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 I
Applicable legislation: —
Status: On the market

Device details

Quantity: 1
Additional product description: Destiné à transvider divers produits. Extérieur bord roulé qui assure une meilleure solidité et évite les déformations.Intérieur avec filtre non amovible, crochet à l'extérieur pour meilleure préhension et suspension. Le tube d'écoulement est conique et présente une déformation dans la masse permettant une régularité dans l'écoulement, pour laisser l'air s'échapper. Il est étroit et peut être utilisé dans les bouteilles. Capacité 0 ,5 ml Ø 150 mm / Capacité 1L Ø 195 mm / Capacité 3L Ø 250 mm
Additional information URL: No additional information URL provided by the manufacturer.
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)03667106000579

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.

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

Critical warnings

No critical warnings reported for this device.

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	—	Still on market

ENTONNOIR

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

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Certificates covering this device

Certificates