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PRIMUS 200 - Indonesia BPOM Medical Device Registration

PRIMUS 200 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201220218. The device is manufactured by CARL ZEISS SUZHOU CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 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.

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BPOM Registered
Risk Class Kelas Resiko : B
PRIMUS 200
Analysis ID: AKL 21201220218

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

CARL ZEISS NEW ZEISS

AR Address

CARL ZEISS INDONESIA

Registration Date

Dec 05, 2022

Expiry Date

Jan 01, 2026

Product Type

Diagnostic Eye Equipment

Optical Coherence Tomography

Non Radiation Electromedics

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