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PREVISCAID Ophthalmic Viscoelastic - Indonesia BPOM Medical Device Registration

PREVISCAID Ophthalmic Viscoelastic is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31204911569. The device is manufactured by MAXIGEN BIOTECH INC., from Taiwan (China), and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. BRIDGE TWO.

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BPOM Registered
Risk Class Kelas Resiko : D
PREVISCAID Ophthalmic Viscoelastic
Analysis ID: AKL 31204911569

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Taiwan (China)

Authorized Representative

PT. BRIDGE TWO

AR Address

Jl. Petojo Melintang No. 17

Registration Date

Aug 12, 2024

Expiry Date

Dec 31, 2027

Product Type

Therapeutic Eye Equipment

Intraocular fluid.

Non Electromedic Sterile

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