Pure Global AI
Philippines FDA registration IVDR-00372

Matrix™ Gel System Diluent - 2 LISS

PhilippinesTulip Diagnostics (P) Ltd. - Gitanjali, Tulip Block, Dr. Antonio Do Rego Bagh, Alto Santacruz, Bambolin Complex P.O., Goa - 403 202, India Mfd by: Tulip Diagnostics (P) Ltd. Plot Nos. 92/96, Phase IIC, Verna Industrial Estate, Verna, Goa - 403 722, India.India.Issued May 26, 2025 – January 30, 2030
VerifiedFDA Philippines · official registry
Device information
Product Name
Matrix™ Gel System Diluent - 2 LISS
Registration Number
IVDR-00372
Manufacturer details
Manufacturer
Tulip Diagnostics (P) Ltd. - Gitanjali, Tulip Block, Dr. Antonio Do Rego Bagh, Alto Santacruz, Bambolin Complex P.O., Goa - 403 202, India Mfd by: Tulip Diagnostics (P) Ltd. Plot Nos. 92/96, Phase IIC, Verna Industrial Estate, Verna, Goa - 403 722, India.
Country of Origin
India.
Importer & distribution
Importer/Distributor
Biosite Medical Instruments
Registration dates
Issuance Date
May 26, 2025
Expiry Date
January 30, 2030
About this record

Access comprehensive regulatory information for Matrix™ Gel System Diluent - 2 LISS in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number IVDR-00372 and manufactured by Tulip Diagnostics (P) Ltd. - Gitanjali, Tulip Block, Dr. Antonio Do Rego Bagh, Alto Santacruz, Bambolin Complex P.O., Goa - 403 202, India Mfd by: Tulip Diagnostics (P) Ltd. Plot Nos. 92/96, Phase IIC, Verna Industrial Estate, Verna, Goa - 403 722, India. in India.. The device was registered on May 26, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Biosite Medical Instruments), 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.