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BIOCLEAR Multi-Purpose Solution with HPMC - Indonesia BPOM Medical Device Registration

BIOCLEAR Multi-Purpose Solution with HPMC is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204918467. The device is manufactured by FORTIS MEDI PHARMACEUTICAL, INC. from Philippines, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GELFLEX VISION INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : C
BIOCLEAR Multi-Purpose Solution with HPMC
Analysis ID: AKL 21204918467

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Philippines

Authorized Representative

PT. GELFLEX VISION INDONESIA

AR Address

JL. AM. SANGAJI NO 17 RT.009/RW.007

Registration Date

Dec 20, 2019

Expiry Date

Oct 21, 2024

Product Type

Therapeutic Eye Equipment

Soft (hydrophilic) contact lens care products.

Non Electromedic Sterile

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