Philippines FDA registration MDR-10328

VACUETTE® TUBE BLOOD COLLECTION TUBE, LH LITHIUM HEPARIN (NON-RIGGED)

Philippines flagPhilippines·Greiner Bio-One GmbH·Thailand·Issued September 22, 2020 – September 22, 2021
Device information
Product Name
VACUETTE® TUBE BLOOD COLLECTION TUBE, LH LITHIUM HEPARIN (NON-RIGGED)
Registration Number
MDR-10328
Manufacturer details
Country of Origin
Thailand
Importer & distribution
Importer/Distributor
Zafire Distributors, Inc.
Registration dates
Issuance Date
September 22, 2020
Expiry Date
September 22, 2021
About this record

Access comprehensive regulatory information for VACUETTE® TUBE BLOOD COLLECTION TUBE, LH LITHIUM HEPARIN (NON-RIGGED) in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10328 and manufactured by Greiner Bio-One GmbH in Thailand. The device was registered on September 22, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Zafire Distributors, 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.

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