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BAERVELDT Glaucoma Implant - Indonesia BPOM Medical Device Registration

BAERVELDT Glaucoma Implant is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21202124232. The device is manufactured by AMO GRONINGEN B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BRIDGE TWO.

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BPOM Registered
Risk Class Kelas Resiko : C
BAERVELDT Glaucoma Implant
Analysis ID: AKL 21202124232

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

AMO GRONINGEN B.V.

Country of Origin

Netherlands

Authorized Representative

PT. BRIDGE TWO

AR Address

Jl. Petojo Melintang No. 17

Registration Date

Sep 10, 2024

Expiry Date

Aug 19, 2027

Product Type

Prosthetic Eye Equipment

Aqueous shunt.

Non Electromedic Sterile

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