Pure Global

EXTARO 300 - Indonesia BPOM Medical Device Registration

EXTARO 300 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603222173. The device is manufactured by CARL ZEISS SUZHOU CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. CARL ZEISS NEW ZEISS.

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 : A
EXTARO 300
Analysis ID: AKL 11603222173

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. CARL ZEISS NEW ZEISS

AR Address

ARKADIA GREEN PARK, TOWER C, LANTAI 12, JL. TB SIMATUPANG KAV. 88

Registration Date

Aug 02, 2023

Expiry Date

Jan 01, 2026

Product Type

Surgical Equipment

Surgical microscope and accessories.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing