Philippines FDA registration MDR-04890

MAXZERO TRI-FUSE EXTENSION SET

Name: MAXZERO TRI-FUSE EXTENSION SET — Philippines FDA registration MDR-04890
Creator: Carefusion Switzerland 317 Sarl
Keywords: MAXZERO TRI-FUSE EXTENSION SET, MDR-04890, Carefusion Switzerland 317 Sarl, Switzerland, Philippines FDA registration

PhilippinesCarefusion Switzerland 317 SarlSwitzerlandIssued October 12, 2017 – January 09, 2022

VerifiedFDA Philippines · official registry

Device information

Product Name: MAXZERO TRI-FUSE EXTENSION SET
Registration Number: MDR-04890

Manufacturer details

Manufacturer: Carefusion Switzerland 317 Sarl
Country of Origin: Switzerland

Importer & distribution

Importer/Distributor

Registration dates

Issuance Date: October 12, 2017
Expiry Date: January 09, 2022

About this record

Access comprehensive regulatory information for MAXZERO TRI-FUSE EXTENSION SET in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-04890 and manufactured by Carefusion Switzerland 317 Sarl in Switzerland. The device was registered on October 12, 2017.

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