Philippines FDA registration MDR-10031

Titanium Ventilation Tube

Name: Titanium Ventilation Tube — Philippines FDA registration MDR-10031
Creator: Spiggle & Theis Medizintechnik GmbH - Burghof 14, 51491 Overath, Germany
Keywords: Titanium Ventilation Tube, MDR-10031, Spiggle & Theis Medizintechnik GmbH - Burghof 14, 51491 Overath, Germany, Josmef Enterprises, Germany, Philippines FDA registration

PhilippinesSpiggle & Theis Medizintechnik GmbH - Burghof 14, 51491 Overath, GermanyGermanyIssued June 08, 2022 – July 23, 2026

VerifiedFDA Philippines · official registry

Device information

Product Name: Titanium Ventilation Tube
Registration Number: MDR-10031

Manufacturer details

Manufacturer: Spiggle & Theis Medizintechnik GmbH - Burghof 14, 51491 Overath, Germany
Country of Origin: Germany

Importer & distribution

Importer/Distributor: Josmef Enterprises

Registration dates

Issuance Date: June 08, 2022
Expiry Date: July 23, 2026

About this record

Access comprehensive regulatory information for Titanium Ventilation Tube in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10031 and manufactured by Spiggle & Theis Medizintechnik GmbH - Burghof 14, 51491 Overath, Germany in Germany. The device was registered on June 08, 2022.

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