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NEXUS Single Vision Lens 1.56 - Indonesia BPOM Medical Device Registration

NEXUS Single Vision Lens 1.56 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11204320671. The device is manufactured by SEE WORLD OPTICAL CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ILT 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
NEXUS Single Vision Lens 1.56
Analysis ID: AKL 11204320671

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. ILT INDONESIA

AR Address

Ruko Mangga Dua Square Blok E No. 16, Jl. Gunung Sahari Raya No.1, Kel. Ancol, Kec. Pademangan, Jakarta Utara

Registration Date

Apr 18, 2023

Expiry Date

Apr 11, 2026

Product Type

Therapeutic Eye Equipment

Prescription show lens.

Non Electromedic Non Sterile

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