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Surestep™ MDMA 500 Urine Drug Test Cassette - FDA Registration IVDR-00740

Access comprehensive regulatory information for Surestep™ MDMA 500 Urine Drug Test Cassette in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00740 and manufactured by Innovacon, Inc. 9975 Summers Ridge Road, San Diego, CA 92121 USA Mfd. By: Abon Biopharm (Hangzhou) Co., Ltd. - #198, 12th Street, East, Hangzhou Economic & Technological Development Area 310018 Hangzhou, People's Republic of China in USA. The device was registered on February 21, 2023.

This page provides complete registration details including manufacturer information, importer/distributor details (Allied Hospital Supply International 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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IVDR-00740
Surestep™ MDMA 500 Urine Drug Test Cassette
Registered medical device in Philippines
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Device Information
Product Name
Surestep™ MDMA 500 Urine Drug Test Cassette
Registration Number
IVDR-00740
Importer & Distribution
Registration Dates
Issuance Date
February 21, 2023
Expiry Date
February 21, 2024