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i-OPTIK Auto Ref Keratometer - ARK 910 - Indonesia BPOM Medical Device Registration

i-OPTIK Auto Ref Keratometer - ARK 910 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201220199. The device is manufactured by NINGBO MING SING OPTICAL R&D CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is UNIVERSAL STAR MULTILINK.

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BPOM Registered
Risk Class Kelas Resiko : A
i-OPTIK Auto Ref Keratometer - ARK 910
Analysis ID: AKL 11201220199

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

UNIVERSAL STAR MULTILINK

AR Address

RUKO SERENADE CENTER BLOK A/27 JL.BOULEVARD GADING SERPONG TANGERANG 15810

Registration Date

Nov 18, 2022

Expiry Date

Nov 23, 2026

Product Type

Diagnostic Eye Equipment

Ophthalmic refractometer.

Non Radiation Electromedics

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