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SR VIVODENT® S PE, SR ORTHOTYP® S PE, SR VIVODENT® S DCL, SR ORTHOTYP® S DCL - DIENTES DE RESINA - INVIMA Registration 1f0d7180d0bab6141051b66db3dadf81

Access comprehensive regulatory information for SR VIVODENT® S PE, SR ORTHOTYP® S PE, SR VIVODENT® S DCL, SR ORTHOTYP® S DCL - DIENTES DE RESINA (SR VIVODENT® S PE, SR ORTHOTYP® S PE, SR VIVODENT® S DCL, SR ORTHOTYP® S DCL - DIENTES DE RESINA) in the Colombia medical device market through Pure Global AI's free database. This IIa medical device is registered under INVIMA analysis ID 1f0d7180d0bab6141051b66db3dadf81 and manufactured by IVOCLAR VIVADENT AG. The device was registered on November 05, 2030.

This page provides complete registration details including product type (SURGICAL DOCTOR), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.

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INVIMA Official Data
IIa
1f0d7180d0bab6141051b66db3dadf81
SR VIVODENT® S PE, SR ORTHOTYP® S PE, SR VIVODENT® S DCL, SR ORTHOTYP® S DCL - DIENTES DE RESINA
INVIMA Analysis ID: 1f0d7180d0bab6141051b66db3dadf81
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Product Use / Uso del Producto
Spanish

LOS DIENTES SR VIVODENT S PE Y SR ORTHOTYP S PE SON USADOS PARA LA FABRICACIÓN DE PRÓTESIS DENTALES.

English

SR VIVODENT S PE AND SR ORTHOTYP S PE TEETH ARE USED FOR THE MANUFACTURE OF DENTAL PROSTHESES.

Device Classification
Risk Class / Clase de Riesgo
IIa
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
1f0d7180d0bab6141051b66db3dadf81
Expire Date
November 05, 2030
Authorized Company / Fabricante
Name (Spanish)
IVOCLAR VIVADENT AG
Name (English)
IVOCLAR VIVADENT AG