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BRIGHTEN OPTIX Ortho-K Overnight Orthokeratology Contact Lens - Indonesia BPOM Medical Device Registration

BRIGHTEN OPTIX Ortho-K Overnight Orthokeratology Contact Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204813330. The device is manufactured by BRIGHTEN OPTIX CORPORATION from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. QUALTEK CONSULTANT JAKARTA.

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BPOM Registered
Risk Class Kelas Resiko : C
BRIGHTEN OPTIX Ortho-K Overnight Orthokeratology Contact Lens
Analysis ID: AKL 21204813330

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

PT. QUALTEK CONSULTANT JAKARTA

AR Address

Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten

Registration Date

Dec 22, 2022

Expiry Date

Dec 15, 2027

Product Type

Therapeutic Eye Equipment

Overnight contact lens orthokeratology

Non Electromedic Non Sterile

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