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WAVELIGHT® Oculyzer II Diagnostic Device - Indonesia BPOM Medical Device Registration

WAVELIGHT® Oculyzer II Diagnostic Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201817819. The device is manufactured by WAVELIGHT GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BINASUKSES CANTEEN.

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Risk Class Kelas Resiko : A
WAVELIGHT® Oculyzer II Diagnostic Device
Analysis ID: AKL 11201817819

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

WAVELIGHT GMBH.

Country of Origin

Germany

Authorized Representative

PT. BINASUKSES CANTEEN

AR Address

Jl. Pulo Kambing II No. 26 Kawasan Industri Pulogadung, Kel. Jatinegara, Kec. Cakung, Kota Adm. Jakarta Timur, Provinsi DKI Jakarta, Kode Pos 13930

Registration Date

Jun 19, 2023

Expiry Date

Jul 01, 2026

Product Type

Diagnostic Eye Equipment

Keratoscope

Non Radiation Electromedics

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