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OPTISOL ™ -GS Corneal Storage Media - Indonesia BPOM Medical Device Registration

OPTISOL ™ -GS Corneal Storage Media is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21202915668. The device is manufactured by ALLIANCE MEDICAL PRODUCTS, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is GLOBAL ALIGNED MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : C
OPTISOL ™ -GS Corneal Storage Media
Analysis ID: AKL 21202915668

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

GLOBAL ALIGNED MEDIKA

AR Address

RUKO PULOGADUNG TRADE CENTRE (PTC) BLOK 8-A NO.7 JL.RAYA BEKASI KM.21 RT.003 RW.003 RAWA TERATE,CAKUNG,JAKARTA TIMUR

Registration Date

Oct 06, 2023

Expiry Date

Aug 02, 2028

Product Type

Prosthetic Eye Equipment

Corneal storage media

Non Electromedic Sterile

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