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HEERA LENS - Indonesia BPOM Medical Device Registration

HEERA LENS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202612001. The device is manufactured by APPASAMY OCULAR DEVICES (P) LTD. from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MEGA MEDICAL ABADI.

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
HEERA LENS
Analysis ID: AKL 31202612001

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

India

Authorized Representative

PT. MEGA MEDICAL ABADI

AR Address

Komplek Fatmawati Mas Blok B5 Kav. 207-208, Jl. RS. Fatmawati No. 20, RT. 005 RW. 010

Registration Date

Jul 29, 2024

Expiry Date

Jun 30, 2029

Product Type

Prosthetic Eye Equipment

Intraocular lens.

Non Electromedic Sterile

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