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OPTOYAG M Medical Therapeutic Laser Device - Indonesia BPOM Medical Device Registration

OPTOYAG M Medical Therapeutic Laser Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203412333. The device is manufactured by OPTOTEK D.O.O. from Slovenia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. EAST RAYA LESTARI.

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 : C
OPTOYAG M Medical Therapeutic Laser Device
Analysis ID: AKL 21203412333

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

OPTOTEK D.O.O.

Country of Origin

Slovenia

Authorized Representative

PT. EAST RAYA LESTARI

AR Address

Jalan Rawa kepiting nomor 4 Kawasan Industri Pulo Gadung Jakarta Timur

Registration Date

Jan 20, 2022

Expiry Date

Nov 24, 2026

Product Type

Surgical Eye Equipment

Nd:YAG laser for posterior capsulotomy and peripheral iridotomy.

Non Radiation Electromedics

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