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SHILEY™ ADULT FLEXIBLE TRACHEOSTOMY TUBE, CUFFLESS DISPOSABLE INNER CANNULA - FDA Registration MDR-10253A

Access comprehensive regulatory information for SHILEY™ ADULT FLEXIBLE TRACHEOSTOMY TUBE, CUFFLESS DISPOSABLE INNER CANNULA in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-10253A and manufactured by Covidien Private Limited in USA. The device was registered on August 19, 2020.

This page provides complete registration details including manufacturer information, importer/distributor details (Medtronic Philippines, 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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USA
MDR-10253A
SHILEY™ ADULT FLEXIBLE TRACHEOSTOMY TUBE, CUFFLESS DISPOSABLE INNER CANNULA
Registered medical device in Philippines
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Device Information
Product Name
SHILEY™ ADULT FLEXIBLE TRACHEOSTOMY TUBE, CUFFLESS DISPOSABLE INNER CANNULA
Registration Number
MDR-10253A
Manufacturer Details
Country of Origin
USA
Importer & Distribution
Importer/Distributor
Medtronic Philippines, Inc.
Registration Dates
Issuance Date
August 19, 2020
Expiry Date
August 19, 2021