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SIDA-LENS PMMA Intraocular Lens - Indonesia BPOM Medical Device Registration

SIDA-LENS PMMA Intraocular Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202714864. The device is manufactured by MOCHINTRA DIANA SIDAPHARM GREECE from Greece, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. TRIUMPHANT MANDARIN OPTO-MEDIC.

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
SIDA-LENS PMMA Intraocular Lens
Analysis ID: AKL 31202714864

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Greece

Authorized Representative

PT. TRIUMPHANT MANDARIN OPTO-MEDIC

AR Address

Jl. Senen Raya No. 135 Ruko Atrium Blok C No. 15 Jakarta Pusat 10410 Tlp : 021-3515478, 3516018 Fax : 021-3511606

Registration Date

Feb 07, 2023

Expiry Date

Jan 23, 2026

Product Type

Prosthetic Eye Equipment

Intraocular lens.

Non Electromedic Sterile

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