MANI Trocar Kit - Infusion Cannula - Indonesia BPOM Medical Device Registration

MANI Trocar Kit - Infusion Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203220202. The device is manufactured by MANI HANOI CO., LTD., PHO YEN FACTORY from Vietnam, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. OPHTHALINDO JAYA MANDIRI.

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BPOM Registered

Risk Class Kelas Resiko : A

MANI Trocar Kit - Infusion Cannula

Analysis ID: AKL 11203220202

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

MANI HANOI CO., LTD., PHO YEN FACTORY

Country of Origin

Vietnam

Authorized Representative

PT. OPHTHALINDO JAYA MANDIRI

AR Address

Superblock Mega Kemayoran (MGK) Blok A No. 8-9 Jl. Angkasa Kav. B-6, Kota Baru, Bandar Kemayoran, Kode Pos 10610, Kel. Gunung Sahari Selatan, Kec. Kemayoran, Kota Jakarta Pusat, Prov. DKI Jakarta