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NATUS Echo-Screen III - Indonesia BPOM Medical Device Registration

NATUS Echo-Screen III is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21001614089. The device is manufactured by CREATION TECHNOLOGIES LP. from Canada, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.

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
NATUS Echo-Screen III
Analysis ID: AKL 21001614089

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Canada

Authorized Representative

PT. IDS MEDICAL SYSTEMS INDONESIA

AR Address

Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410

Registration Date

Dec 18, 2023

Expiry Date

Nov 30, 2028

Product Type

Diagnostic Neurology Equipment

Evoked response auditory stimulator.

Non Radiation Electromedics

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