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NIDEK Optical Coherence Tomoghraphy - Indonesia BPOM Medical Device Registration

NIDEK Optical Coherence Tomoghraphy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201420194. The device is manufactured by NIDEK CO.,LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MULYA HUSADA JAYA.

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BPOM Registered
Risk Class Kelas Resiko : B
NIDEK Optical Coherence Tomoghraphy
Analysis ID: AKL 21201420194

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

NIDEK CO.,LTD.

Country of Origin

Japan

Authorized Representative

MULYA HUSADA JAYA

AR Address

JALAN KERINCI NO. 2-A

Registration Date

Oct 25, 2024

Expiry Date

Jun 10, 2029

Product Type

Diagnostic Eye Equipment

Ophthalmoscope.

Non Radiation Electromedics

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