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PEG-24-PULL PERCUTANEUOS ENDOSCOPIC GASTROSTOMY TUBE - FDA Registration DVR-7382

Access comprehensive regulatory information for PEG-24-PULL PERCUTANEUOS ENDOSCOPIC GASTROSTOMY TUBE in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number DVR-7382 and manufactured by Cook Medical Australia Pty Ltd. - 95 Brandl Street Eight Mile Plains, Queensland, Australia 4113 Mfd by: Wilson-Cook Medical, Inc. - 4900 Bethania Station Road, Winston-Salem, North Carolina, USA in USA. The device was registered on August 06, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Macare Medicals, 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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DVR-7382
PEG-24-PULL PERCUTANEUOS ENDOSCOPIC GASTROSTOMY TUBE
Registered medical device in Philippines
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Device Information
Product Name
PEG-24-PULL PERCUTANEUOS ENDOSCOPIC GASTROSTOMY TUBE
Registration Number
DVR-7382
Importer & Distribution
Importer/Distributor
Macare Medicals, Inc.
Registration Dates
Issuance Date
August 06, 2024
Expiry Date
June 17, 2029