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ASSURA® / ALTERNA® POST-OP OSTOMY BAG, 1-PIECE OPEN WITH INSPECTION WINDOW, TRANSPARENT - FDA Registration MDR-06690

Access comprehensive regulatory information for ASSURA® / ALTERNA® POST-OP OSTOMY BAG, 1-PIECE OPEN WITH INSPECTION WINDOW, TRANSPARENT in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-06690 and manufactured by Coloplast (Hongkong) Ltd. in Hungary. The device was registered on April 10, 2019.

This page provides complete registration details including manufacturer information, importer/distributor details (Completesolution Pharmacy & General Merchandise), 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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Hungary
MDR-06690
ASSURA® / ALTERNA® POST-OP OSTOMY BAG, 1-PIECE OPEN WITH INSPECTION WINDOW, TRANSPARENT
Registered medical device in Philippines
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Device Information
Product Name
ASSURA® / ALTERNA® POST-OP OSTOMY BAG, 1-PIECE OPEN WITH INSPECTION WINDOW, TRANSPARENT
Registration Number
MDR-06690
Manufacturer Details
Country of Origin
Hungary
Importer & Distribution
Registration Dates
Issuance Date
April 10, 2019
Expiry Date
April 24, 2024