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NIDEK Auto Ref/Keratometer / Auto Refractometer - Indonesia BPOM Medical Device Registration

NIDEK Auto Ref/Keratometer / Auto Refractometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201916856. The device is manufactured by NIDEK CO., LTD., HAMACHO PLANT from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MULYA HUSADA JAYA.

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BPOM Registered
Risk Class Kelas Resiko : A
NIDEK Auto Ref/Keratometer / Auto Refractometer
Analysis ID: AKL 11201916856

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Japan

Authorized Representative

MULYA HUSADA JAYA

AR Address

JALAN KERINCI NO. 2-A

Registration Date

Mar 28, 2024

Expiry Date

Mar 31, 2028

Product Type

Diagnostic Eye Equipment

Ophthalmic refractometer.

Non Radiation Electromedics

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