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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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Organization name
UDI-DI code
Reference / catalog number

DRUG SPRAYING CANNULAS — Class I MDR by Laboratoire Aguettant

MD Atlas
Laboratoire Aguettant

EUDAMED last updated this device on Aug 4, 2025

DRUG SPRAYING CANNULAS

37005677CANULEEX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Laboratoire Aguettant
UDI-DI code: 03700567702573
Reference / catalog number: 64252

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Manufacturer information

Organization name: Laboratoire Aguettant
SRN: FR-MF-000000509
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: DRUG SPRAYING CANNULAS
UDI-DI code: 03700567702573
Basic UDI-DI: 37005677CANULEEX
Reference / catalog number: 64252
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 8
Additional product description: Drug spraying Cannulas are intended to be used as a tool to spray a drug in the mouth area in order to perform a local anesthesia, for example before intubation or before minor ENT (Ear Nose Throat) surgeries. They are intended to be used with LIDOCAINE AGUETTANT 5% solution for oral spraying
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A13APPLICATORS FOR DRUGS AND MEDICAL DEVICES NOT PRESENT IN OTHER CLASSES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

BIDON EAU STERILE 5L37005677BIDON-EAU26On the market BLUE MARKER AGUETTANT®B-FRMF-000000509-6006747LOn the market BLUE MARKER AGUETTANT®B-FRMF-000000509-6009377VOn the market DRUG SPRAYING CANNULAS37005677CANULEEXOn the market DRUG SPRAYING CANNULAS37005677CANULEEXOn the market

Certificates

No 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.