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ERK-9000 Autorefractor/Keratometer - Indonesia BPOM Medical Device Registration

ERK-9000 Autorefractor/Keratometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201711691. The device is manufactured by U.S OPHTHALMIC LLC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PRIMARY WORKS.

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BPOM Registered
Risk Class Kelas Resiko : A
ERK-9000 Autorefractor/Keratometer
Analysis ID: AKL 11201711691

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

PT. PRIMARY WORKS

AR Address

Daan Mogot Arcadia Blok F.1/8A-8B Jl. Daan Mogot Km 21, Kelurahan Batu Ceper

Registration Date

Mar 22, 2022

Expiry Date

Oct 28, 2025

Product Type

Diagnostic Eye Equipment

Ophthalmic refractometer.

Non Radiation Electromedics

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