Pure Global

AT TORBI 709 M - Indonesia BPOM Medical Device Registration

AT TORBI 709 M is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202313543. The device is manufactured by CARL ZEISS MEDITEC AG. from Germany, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is ELO KARSA UTAMA.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : D
AT TORBI 709 M
Analysis ID: AKL 31202313543

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Germany

Authorized Representative

ELO KARSA UTAMA

AR Address

Jl. Raya Kebayoran Lama No. 34-E, Grogol Selatan, Kebayoran Lama.

Registration Date

Mar 05, 2022

Expiry Date

May 01, 2025

Product Type

Prosthetic Eye Equipment

Intraocular lens.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing