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PHACER - Indonesia BPOM Medical Device Registration

PHACER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201320333. The device is manufactured by TAIYUAN NORTH CHINA XINYUAN TECH CENTER(CO.,LTD) from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ATALLA NEW Zealand.

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
PHACER
Analysis ID: AKL 11201320333

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. ATALLA NEW Zealand

AR Address

JL.PUTRA I NO.33 A, KAWASAN INDUSTRI PASAR KEMIS

Registration Date

Jun 19, 2023

Expiry Date

May 09, 2025

Product Type

Diagnostic Eye Equipment

Ophthalmic refractometer.

Non Radiation Electromedics

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