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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

SEQUENCEUR MF UDMA VIOLET… — Class IIa MDD by Exotec Dentaire

MD Atlas
Exotec Dentaire

EUDAMED last updated this device on May 10, 2026

SEQUENCEUR MF UDMA VIOLET CORPORIS (1 FORET)

B-+D055TE001520

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Exotec Dentaire
UDI-DI code: +D055TE001520
Reference / catalog number: TE00152

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Manufacturer information

Organization name: Exotec Dentaire
SRN: FR-MF-000004026
Manufacturer status: Active

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SEQUENCEUR RC TITANE JAUNE CORPORIS(1 FORET)B-+D055TE001010On the market ALESOIR CORPORIS BLEU(x1)[FR]B-+D055TE010131On the market ALESOIR CORPORIS BLEU(X3)[FR]B-+D055TE011131On the market ALESOIR CORPORIS GRIS(X1)[FR]B-+D055TE010141On the market ALESOIR CORPORIS GRIS(X3)[FR]B-+D055TE011141On 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.

Critical warnings

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

CW010
Afin d'éviter tout risque infectieux et d'utilisation,respecter le protocole de nettoyage et de stérilisation recommandé ainsi que les instructions d'utilisation
CW011
La décision finale de réaliser un acte RCR relève de la décision clinique du professionnel de santé en fonction du cas clinique

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Feb 28, 2018	May 10, 2026

Device identification

Trade name: SEQUENCEUR MF UDMA VIOLET CORPORIS (1 FORET)
UDI-DI code: +D055TE001520
Basic UDI-DI: B-+D055TE001520
Reference / catalog number: TE00152
Issuing entity: HIBCC

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Système METAL-FREE UDMA (MF UDMA) : Tenons translucides radio-opaques en fibre de verre et matrice polymère à base de résine UDMA (uréthane diméthacrylate) ; ne contiennent pas de BisGMA
Additional information URL: https://www.exotec-dentaire.com/Product/FamilyAndProduct
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q010199CONSERVATIVE DENTISTRY AND ENDODONTICS DEVICES - OTHER

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
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Software identification