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ARTERIAL-VENOUS FISTULA SET (Rotating Wing) - FDA Registration ef992b911d8cc733647df53c7c6a199c

Access comprehensive regulatory information for ARTERIAL-VENOUS FISTULA SET (Rotating Wing) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ef992b911d8cc733647df53c7c6a199c and manufactured by Hospitech Manufacturing Services Sdn. Bhd.. The device was registered on August 16, 2022.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.

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FDA Official Data
ef992b911d8cc733647df53c7c6a199c
ARTERIAL-VENOUS FISTULA SET (Rotating Wing)
FDA ID: ef992b911d8cc733647df53c7c6a199c
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Device Classification
Brand Name
SATORI
Registration Information
Analysis ID
ef992b911d8cc733647df53c7c6a199c
Registration Date
August 16, 2022