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MAIN MEDITECH Non-Mydiatric Automatic Fundus Camera - Indonesia BPOM Medical Device Registration

MAIN MEDITECH Non-Mydiatric Automatic Fundus Camera is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201220173. The device is manufactured by CHONGQING BIO NEW VISION MEDICALEQUIPMENT CO.,LTD from China, 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
MAIN MEDITECH Non-Mydiatric Automatic Fundus Camera
Analysis ID: AKL 21201220173

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. TRIASTRI MEDITAMA

AR Address

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

Registration Date

Oct 21, 2022

Expiry Date

Jul 31, 2027

Product Type

Diagnostic Eye Equipment

Opthalmic camera.

Non Radiation Electromedics

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