Philippines FDA registration MDR-01221

Airlife™ Prefilled Humidifier with Sterile Water for Inhalation 500ml USP with Adapter

Philippines flagPhilippines·Vital Signs,Inc.- Princeton South Corporate Center, 100 Charles Ewing Blvd., Suite 160, Ewing New Jersey, USA Mfd by: Productos Urologos de Mexico S.A. De C.V- Cerrada via de la Produccion No. 85 Parque Industrial Mexicali III Baja California, Mexico·Mexico·Issued August 02, 2024 – May 07, 2029
Device information
Product Name
Airlife™ Prefilled Humidifier with Sterile Water for Inhalation 500ml USP with Adapter
Registration Number
MDR-01221
Manufacturer details
Country of Origin
Mexico
Importer & distribution
Importer/Distributor
Lifelink, Inc.
Registration dates
Issuance Date
August 02, 2024
Expiry Date
May 07, 2029
About this record

Access comprehensive regulatory information for Airlife™ Prefilled Humidifier with Sterile Water for Inhalation 500ml USP with Adapter in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01221 and manufactured by Vital Signs,Inc.- Princeton South Corporate Center, 100 Charles Ewing Blvd., Suite 160, Ewing New Jersey, USA Mfd by: Productos Urologos de Mexico S.A. De C.V- Cerrada via de la Produccion No. 85 Parque Industrial Mexicali III Baja California, Mexico in Mexico. The device was registered on August 02, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Lifelink, Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.

Free DatabasePowered by Pure Global AIFDA Official DataMexico