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AJL-VISC Sodium Hyaluronate Viscoelastic Solution - Indonesia BPOM Medical Device Registration

AJL-VISC Sodium Hyaluronate Viscoelastic Solution is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203220024. The device is manufactured by AJL OPHTHALMIC S.A. from Spain, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. SOCA MEDIKA 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 : D
AJL-VISC Sodium Hyaluronate Viscoelastic Solution
Analysis ID: AKL 31203220024

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Spain

Authorized Representative

PT. SOCA MEDIKA INDONESIA

AR Address

Pulogadung Trade Center Blok 8 C No. 5, Jl. Raya Bekasi KM 21

Registration Date

Mar 06, 2024

Expiry Date

Feb 06, 2029

Product Type

Surgical Eye Equipment

Intraocular fluid.

Non Electromedic Sterile

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