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Philippines FDA registration CMDR-2022-00493A

Terumo Destination Peripheral Guiding Sheath with CCV

PhilippinesTerumo Medical Corporation - 265 Davidson Ave., Suite 320, Somerset, New Jersey USA mfd. By: Terumo Marketing Corporation - 950 Elkton Blvd. Elkton, Maryland, USAUSAIssued May 05, 2022 – May 05, 2027
VerifiedFDA Philippines · official registry
Device information
Product Name
Terumo Destination Peripheral Guiding Sheath with CCV
Registration Number
CMDR-2022-00493A
Manufacturer details
Country of Origin
USA
Importer & distribution
Registration dates
Issuance Date
May 05, 2022
Expiry Date
May 05, 2027
About this record

Access comprehensive regulatory information for Terumo Destination Peripheral Guiding Sheath with CCV in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2022-00493A and manufactured by Terumo Medical Corporation - 265 Davidson Ave., Suite 320, Somerset, New Jersey USA mfd. By: Terumo Marketing Corporation - 950 Elkton Blvd. Elkton, Maryland, USA in USA. The device was registered on May 05, 2022.

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