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Tuta Burette Set - FDA Registration CMDR-2024-03158

Access comprehensive regulatory information for Tuta Burette Set in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-03158 and manufactured by ICU Medical Australia Pty Ltd. - Unit U, 10-16 South St Rydalmere New South Wales 2116 Australia Mfd by: Amsino Medical (Kunshan) Co., Ltd. - 582 Lidu Road, Qiandeng Town 215343 Kunshan City PR, China in CHINA. The device was registered on August 09, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (East Lane Corporation), 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.

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CMDR-2024-03158
Tuta Burette Set
Registered medical device in Philippines
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Device Information
Product Name
Tuta Burette Set
Registration Number
CMDR-2024-03158
Importer & Distribution
Importer/Distributor
East Lane Corporation
Registration Dates
Issuance Date
August 09, 2024
Expiry Date
August 09, 2029