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KOWA NONMYD BY - Indonesia BPOM Medical Device Registration

KOWA NONMYD BY is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201023915. The device is manufactured by KOWA COMPANY LTD, CHOFU FACTORY from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRIASTRI MEDITAMA.

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BPOM Registered
Risk Class Kelas Resiko : B
KOWA NONMYD BY

KOWA NONMYD AF

Analysis ID: AKL 21201023915

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. TRIASTRI MEDITAMA

AR Address

GRIYA KEMAYORAN BLOK R-41 JL. INDUSTRI RAYA NO. 9-11

Registration Date

Dec 13, 2021

Expiry Date

Dec 13, 2026

Product Type

Diagnostic Eye Equipment

Opthalmic camera.

Non Radiation Electromedics

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