Philippines FDA registration MDR-05796H

BIOTEQ® Precision Infusion Set, Air-Vented Spike, Needleless Type Y-Connector

Philippines flagPhilippines·Bioteque Medical Phil. Inc.·Philippines·Issued February 06, 2025 – July 12, 2028
Device information
Product Name
BIOTEQ® Precision Infusion Set, Air-Vented Spike, Needleless Type Y-Connector
Registration Number
MDR-05796H
Manufacturer details
Country of Origin
Philippines
Importer & distribution
Importer/Distributor
n/a
Registration dates
Issuance Date
February 06, 2025
Expiry Date
July 12, 2028
About this record

Access comprehensive regulatory information for BIOTEQ® Precision Infusion Set, Air-Vented Spike, Needleless Type Y-Connector in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05796H and manufactured by Bioteque Medical Phil. Inc. in Philippines. The device was registered on February 06, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (n/a), 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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