EUDAMED last updated this device on Apr 24, 2026

ALESOIR CORPORIS JAUNE (X1)

B-+D055TE010111

On the marketClass IIa

Applicable legislation: —
Organization name: Exotec Dentaire
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 →: +D055TE010111
Reference / catalog number: TE01011

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.

ALESOIR CORPORIS JAUNE (X1) is an EU-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Exotec Dentaire. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: ALESOIR CORPORIS JAUNE (X1)
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 →: +D055TE010111
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 →: B-+D055TE010111
Reference / catalog number: TE01011
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 →: HIBCC

Classification

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

Device details

Quantity: 1
Additional product description: Les forets et alésoirs sont destinés à la mise en forme de la racine (alésage/forage) d’une dent dépulpée de manière à créer le logement pour un tenon radiculaire.
Additional information URL: https://www.exotec-dentaire.com/Product/FamilyAndProduct
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

+D055TE010111

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

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EMDN nomenclature code(s)

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

L159099ODONTOSTOMATOLOGY INSTRUMENTS, REUSABLE - OTHER

Critical warnings

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

Caution
La décision finale de réaliser un acte RCR relève de la décision clinique du professionnel de santé en fonction du cas clinique
Consult instructions for use
Afin d'éviter tout risque infectieux et d’utilisation, respecter le protocole de nettoyage et de stérilisation recommandé ainsi que les instructions d’utilisation.

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	Feb 26, 2019	Apr 24, 2026

ALESOIR CORPORIS JAUNE (X1)

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Device details

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UDI-DI DataMatrix

EMDN nomenclature code(s)

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Market distribution

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Device identification

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Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

EMDN nomenclature code(s)

Critical warnings

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Safety

Regulatory

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Certificates

Legacy certificates

Certificates covering this device

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Certificates covering this device

Legacy certificates

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