NIPRO ARTERIAL VENOUS FISTULA NEEDLE (NIPRO VENOUS ARTERY FISTULA NEEDLE). - DIGEMID Registration DM3636E
Access comprehensive regulatory information for NIPRO ARTERIAL VENOUS FISTULA NEEDLE (NIPRO VENOUS ARTERY FISTULA NEEDLE). in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DM3636E and manufactured by NIPRO (THAILAND) CORPORATION LIMITED. The device was registered on December 06, 2013.
This page provides complete registration details including product type (MEDICAL DEVICE), manufacturer information, authorized representative details, and regulatory compliance data from the official Peru DIGEMID medical device database. Pure Global AI offers free access to Peru's complete medical device registry.
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DIGEMID Official Data
DM3636E
NIPRO ARTERIAL VENOUS FISTULA NEEDLE (NIPRO VENOUS ARTERY FISTULA NEEDLE).
DIGEMID ID: DM3636E
Local name: NIPRO ARTERIAL VENOUS FISTULA NEEDLE (AGUJA PARA FISTULA ARTERIO VENOSA NIPRO).
Device Classification
Product Type
MEDICAL DEVICE
Registration Information
Analysis ID
DM3636E
Registration Date
December 06, 2013
Expiration Date
December 05, 2028
Creation Date
January 13, 2025
Manufacturer
Authorized Representative

