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ESSILOR OPTHALMOSCOPE - Indonesia BPOM Medical Device Registration

ESSILOR OPTHALMOSCOPE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201320371. The device is manufactured by KEELER LTD from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is OPTICAL PARTNERS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
ESSILOR OPTHALMOSCOPE
Analysis ID: AKL 21201320371

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

KEELER LTD

Country of Origin

United Kingdom

Authorized Representative

OPTICAL PARTNERS INDONESIA

AR Address

JL. TOMANG RAYA NO 15A, TOMANG GROGOL PETAMBURAN

Registration Date

Sep 29, 2023

Expiry Date

Jan 31, 2028

Product Type

Diagnostic Eye Equipment

Ophthalmoscope.

Non Radiation Electromedics

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