MANI Ophthalmic Sutures PGA - Indonesia BPOM Medical Device Registration
MANI Ophthalmic Sutures PGA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603611494. The device is manufactured by MANI, INC. KIYOHARA FACTORY from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. OPHTHALINDO JAYA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
MANI, INC. KIYOHARA FACTORYCountry of Origin
Japan
Authorized Representative
PT. OPHTHALINDO JAYAAR Address
KOMPLEK KEMAYORAN MEGA GLODOK, BLOK A NO.8, GUNUNG SEHARI SELATAN
Registration Date
Dec 29, 2020
Expiry Date
Dec 31, 2023
Product Type
Surgical Equipment
Absorbable poly(glycolide/ l -lactide) surgical suture.
Non Electromedic Sterile
MANI Ophthalmic Sutures - Polyester
MANI HANOI CO., LTD. PHO YEN 2 FACTORY
MANI Ophthalmic Sutures - Nylon
MANI HANOI CO., LTD, PHO YEN 2 FACTORY
MANI Ophthalmic Sutures - Polypropylene
MANI HANOI CO., LTD. PHO YEN 2 FACTORY
MANI Ophthalmic Sutures - Silk
MANI HANOI CO., LTD. PHO YEN 2 FACTORY
MANI Swap Kit
MANI, INC., KIYOHARA FACTORY
MANI Infusion Cannula Trocar Kit
MANI, INC., KIYOHARA FACTORY