Flouroplastic (PTFE) Ventilation Tube
Philippines·Spiggle & Theis Medizintechnik GmbH Burghof 14, 51491 Overath, Germany·Germany·Issued October 20, 2022 – July 23, 2026- Product Name
- Flouroplastic (PTFE) Ventilation Tube
- Registration Number
- MDR-10030
- Country of Origin
- Germany
- Importer/Distributor
- josmef Medical Corporation
- Issuance Date
- October 20, 2022
- Expiry Date
- July 23, 2026
Access comprehensive regulatory information for Flouroplastic (PTFE) Ventilation Tube in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10030 and manufactured by Spiggle & Theis Medizintechnik GmbH Burghof 14, 51491 Overath, Germany in Germany. The device was registered on October 20, 2022.
This page provides complete registration details including manufacturer information, importer/distributor details (josmef Medical Corporation), 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.