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FSV PENTAX AS 1.55 REFINE INC - Indonesia BPOM Medical Device Registration

FSV PENTAX AS 1.55 REFINE INC is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11204420422. The device is manufactured by VIVO OPTICS CO.,LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. HOYA LENS 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 : A
FSV PENTAX AS 1.55 REFINE INC
Analysis ID: AKL 11204420422

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. HOYA LENS INDONESIA

AR Address

Wisma Lumbini , Lt3 , Jl Tomang Raya no:53 , Tomang ,Jakarta barat 11440

Registration Date

Sep 10, 2024

Expiry Date

May 31, 2028

Product Type

Therapeutic Eye Equipment

Prescription show lens.

Non Electromedic Non Sterile

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