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ESSILOR MYOPIA EXPERT 700 - Indonesia BPOM Medical Device Registration

ESSILOR MYOPIA EXPERT 700 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21202420028. The device is manufactured by VISIA IMAGING S.R.L from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is OPTICAL PARTNERS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
ESSILOR MYOPIA EXPERT 700
Analysis ID: AKL 21202420028

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

OPTICAL PARTNERS INDONESIA

AR Address

JL. TOMANG RAYA NO 15A, TOMANG GROGOL PETAMBURAN

Registration Date

Apr 17, 2024

Expiry Date

Nov 02, 2028

Product Type

Prosthetic Eye Equipment

Keratoprosthesis.

Non Radiation Electromedics

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