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miLOOP - Indonesia BPOM Medical Device Registration

miLOOP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203220051. The device is manufactured by CARL ZEISS MEDITEC CATARACT TECHNOLOGY INC. from United States, 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.

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BPOM Registered
Risk Class Kelas Resiko : A
miLOOP
Analysis ID: AKL 11203220051

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

PT. CARL ZEISS NEW ZEISS

AR Address

CARL ZEISS INDONESIA

Registration Date

Jun 30, 2022

Expiry Date

Sep 30, 2026

Product Type

Surgical Eye Equipment

Manual ophthalmic surgical instrument.

Non Electromedic Sterile

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