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ZEISS MEL 90 - Indonesia BPOM Medical Device Registration

ZEISS MEL 90 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203320410. The device is manufactured by CARL ZEISS MEDITEC AG (CARL-ZEISS-PROMENADE) from Germany, and is classified as Risk Class Kelas Resiko : C. 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.

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BPOM Registered
Risk Class Kelas Resiko : C
ZEISS MEL 90
Analysis ID: AKL 21203320410

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. CARL ZEISS NEW ZEISS

AR Address

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

Registration Date

Oct 23, 2023

Expiry Date

Sep 30, 2026

Product Type

Surgical Eye Equipment

Excimer laser system

Non Radiation Electromedics

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