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CLAIRLUX Resin Lens - Indonesia BPOM Medical Device Registration

CLAIRLUX Resin Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11204420073. The device is manufactured by ZHEJIANG WEIXING OPTICAL CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. INDOMATA OPTICAL PARTNERS.

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BPOM Registered
Risk Class Kelas Resiko : A
CLAIRLUX Resin Lens
Analysis ID: AKL 11204420073

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. INDOMATA OPTICAL PARTNERS

AR Address

Tamini Square Lt. Dasar, Jl. Raya Taman MII Blok GS-39 No. 5 Rt 003 Rw 002, Prov. DKI Jakarta, Kota Jakarta Timur, Kec. Makasar, Kel. Pinangranti

Registration Date

Feb 06, 2024

Expiry Date

Feb 05, 2027

Product Type

Therapeutic Eye Equipment

Prescription show lens.

Non Electromedic Non Sterile

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