Argentina flag640-279

FIBERGLASS POSTS

POSTES DE FIBRA DE VIDRIO

Argentina Medical Device Registration · SUPERDONT · CALAMANTE HORACIO R. AND CALAMANTE N.G. · Registered May 13, 2024

Class I-II Registration
Device classification
Registration Type
Class I-II Registration
Registro Clase I-II
Product Code
640-279
Brand Name
SUPERDONT
Product Name
FIBERGLASS POSTS
POSTES DE FIBRA DE VIDRIO
Registration information
Registration Date
May 13, 2024
Database ID
cmhayu0e20euuekuze0udiqt9
Authorized representative
Name
CALAMANTE HORACIO R. AND CALAMANTE N.G.
CALAMANTE HORACIO R. Y CALAMANTE N.G.
Documents
Product information

SUPERPOST+: (SPLC 2+) LIGHTCORE+2, (SPLC 3+) LIGHTCORE+3, (SPNF 0+) NANOFINE+0, (SPNF 1+) NANOFINE+1, (SPNF 2+) NANOFINE+2, (SPUF 0+) ULTRAFINO+0, (SPUF 1+) ULTRAFINO+1, (SPUF 2+) ULTRAFINO+2, (SPRT 0,5) RT MAX 0,5, (SPRT 1) RT MAX 1, (SPRT 2) RT MAX 2, (SPLM 0,5) LISO MAX 0,5, (SPLM 1) LISO MAX 1, (SPLM 2) LISO MAX 2, (SPG 1+) ESTRIADO+1, (SPG 2+) ESTRIADO+2, (SPG 3+ ) ESTRIADO+3, (SPL 0,5+) Liso+ 0,5 (SPL1+) Liso+ 1, (SPL 2+) Liso+ 2, (SPL 3+) Liso+ 3, (SPLB 1+) LIGHTBALL+1, ( SPLB 2+) LIGHTBALL+2, (SPLB3+) LIGHTBALL+3, (SPLC 1+) LIGHTCORE+1

Spanish:

SUPERPOST+: (SPLC 2+) LIGHTCORE+2, (SPLC 3+) LIGHTCORE+3, (SPNF 0+) NANOFINE+0, (SPNF 1+) NANOFINE+1, (SPNF 2+) NANOFINE+2, (SPUF 0+) ULTRAFINO+0, (SPUF 1+) ULTRAFINO+1, (SPUF 2+) ULTRAFINO+2, (SPRT 0,5) RT MAX 0,5, (SPRT 1) RT MAX 1, (SPRT 2) RT MAX 2, (SPLM 0,5) LISO MAX 0,5, (SPLM 1) LISO MAX 1, (SPLM 2) LISO MAX 2, (SPG 1+) ESTRIADO+1, (SPG 2+) ESTRIADO+2, (SPG 3+ ) ESTRIADO+3, (SPL 0,5+) Liso+ 0,5 (SPL1+) Liso+ 1, (SPL 2+) Liso+ 2, (SPL 3+) Liso+ 3, (SPLB 1+) LIGHTBALL+1, ( SPLB 2+) LIGHTBALL+2, (SPLB3+) LIGHTBALL+3, (SPLC 1+) LIGHTCORE+1

About this record

Access comprehensive regulatory information for FIBERGLASS POSTS in the Argentina medical device market through Pure Global AI's free database. This Class I-II Registration medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on May 13, 2024.

This page provides complete registration details including product code (640-279), brand name (SUPERDONT), authorized representative information, registration type, and regulatory compliance data from the official Argentina ANMAT medical device database. Pure Global AI offers free access to Argentina's medical device registry, helping global MedTech companies navigate Argentina regulations efficiently.

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