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Probe - Argentina Medical Device Registration

Access comprehensive regulatory information for Probe in the Argentina medical device market through Pure Global AI's free database. This Revalidation of Registration I-II-III-IV medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on December 18, 2023.

This page provides complete registration details including product code (648-33), brand name (Freka), 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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Argentina ANMAT Data
Bilingual (Spanish/English)
Revalidation of Registration I-II-III-IV
Probe
Sonda
Argentina Medical Device Registration
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Product Information

1) Freka FR 8 probe, 120 cm, ENFit (7981827) 2) Freka FR 10 probe, 120 cm, ENFit (7981828) 3) Freka FR 12 probe, 120 cm, ENFit (7981829) 4) Freka FR 8 linear probe, 120 cm, ENFit (7981840) 5) Freka FR 10 linear probe, 120 cm, ENFit (7981842) 6) Freka FR 12 linear probe, 120 cm, ENFit (7981843) 7) Freka FR 15 linear probe, 120 cm, ENFit (7981844)

Spanish:

1) Sonda Freka FR 8, 120 cm, ENFit (7981827) 2) Sonda Freka FR 10, 120 cm, ENFit (7981828) 3) Sonda Freka FR 12, 120 cm, ENFit (7981829) 4) Sonda Freka FR 8 lineal, 120 cm, ENFit (7981840) 5) Sonda Freka FR 10 lineal, 120 cm, ENFit (7981842) 6) Sonda Freka FR 12 lineal, 120 cm, ENFit (7981843) 7) Sonda Freka FR 15 lineal, 120 cm, ENFit (7981844)

Device Classification
Registration Type
Revalidation of Registration I-II-III-IV
Revรกlida de Registro I-II-III-IV
Product Code
648-33
Brand Name
Freka
Product Name
Probe
Sonda
Registration Information
Registration Date
December 18, 2023
Database ID
cmhaytwgm0bvnekuzggdvie6v
Authorized Representative