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Infivision ET1000 - Indonesia BPOM Medical Device Registration

Infivision ET1000 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401420043. The device is manufactured by INFIVISION MEDICAL IMAGING TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. INDOMEDIK NIAGA PERKASA.

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
Infivision ET1000
Analysis ID: AKL 20401420043

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INDOMEDIK NIAGA PERKASA

AR Address

JALAN RAYA KEBAYORAN LAMA NO.35 RT.008 RW.001 Kel. Sukabumi Selatan Kec, Kebon Jeruk, Jakarta Barat, provinsi DKI Jakarta

Registration Date

Oct 07, 2024

Expiry Date

Dec 31, 2027

Product Type

Diagnostic Anesthesia Equipment

Ventilatory electrical impedance tomograph

Non Radiation Electromedics

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