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MANI® OPTHALMIC KNIFE, GOLF/SCLERAL - FDA Registration MDR-05086G

Access comprehensive regulatory information for MANI® OPTHALMIC KNIFE, GOLF/SCLERAL in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-05086G and manufactured by Mani Inc. 8-3 Kiyohara Industrial Park Utsunomiya, Tochigi, Japan Mfd. By: Mani Hanoi Co., Ltd. Pho Yen Factory - vang Residential Group, Tan Huong Ward, Pho Yen City, Thai Nguyen Province, Vietnam in Japan. The device was registered on January 24, 2023.

This page provides complete registration details including manufacturer information, importer/distributor details (I-Senz Medical, 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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Japan
MDR-05086G
MANI® OPTHALMIC KNIFE, GOLF/SCLERAL
Registered medical device in Philippines
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Device Information
Product Name
MANI® OPTHALMIC KNIFE, GOLF/SCLERAL
Registration Number
MDR-05086G
Importer & Distribution
Importer/Distributor
I-Senz Medical, Inc.
Registration Dates
Issuance Date
January 24, 2023
Expiry Date
January 25, 2028