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MORIA EVOLUTION 3E Microkeratome System - Indonesia BPOM Medical Device Registration

MORIA EVOLUTION 3E Microkeratome System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203024651. The device is manufactured by MORIA S.A. from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. KATAMATA OPTOMEDIK.

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Risk Class Kelas Resiko : A
MORIA EVOLUTION 3E Microkeratome System
Analysis ID: AKL 11203024651

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

MORIA S.A.

Country of Origin

France

Authorized Representative

PT. KATAMATA OPTOMEDIK

AR Address

Komplek Ketapang Indah Blok B2 No.31 Jl. KH. Zainul Arifin Kel.Krukut, Kec.Taman Sari Jakarta Barat

Registration Date

Aug 18, 2020

Expiry Date

Dec 21, 2024

Product Type

Surgical Eye Equipment

Keratome.

Non Radiation Electromedics

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