RESPIRATORY HUMIDIFIER; VENTED AUTOFEED HUMIDIFICATION CHAMBER; REUSABLE HUMIDIFICATION CHAMBER. - DIGEMID Registration DM12975E
Access comprehensive regulatory information for RESPIRATORY HUMIDIFIER; VENTED AUTOFEED HUMIDIFICATION CHAMBER; REUSABLE HUMIDIFICATION CHAMBER. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DM12975E and manufactured by FISHER & PAYKEL HEALTHCARE LIMITED. The device was registered on January 08, 2017.
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
DM12975E
RESPIRATORY HUMIDIFIER; VENTED AUTOFEED HUMIDIFICATION CHAMBER; REUSABLE HUMIDIFICATION CHAMBER.
DIGEMID ID: DM12975E
Device Classification
Product Type
MEDICAL DEVICE
Registration Information
Analysis ID
DM12975E
Registration Date
January 08, 2017
Expiration Date
January 08, 2022
Creation Date
February 23, 2023
Manufacturer
Authorized Representative
Name
CEPCO S.A.C.
