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CATARHEX 3 Phacoemulsifiication System - Indonesia BPOM Medical Device Registration

CATARHEX 3 Phacoemulsifiication System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203912112. The device is manufactured by OERTLI INSTRUMENTE AG. from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KATAMATA OPTOMEDIK.

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BPOM Registered
Risk Class Kelas Resiko : C
CATARHEX 3 Phacoemulsifiication System
Analysis ID: AKL 21203912112

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Switzerland

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

Jul 06, 2023

Expiry Date

Dec 05, 2027

Product Type

Surgical Eye Equipment

Phacofragmentation system.

Non Radiation Electromedics

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