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HEYER Vaporizer - Indonesia BPOM Medical Device Registration

HEYER Vaporizer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403121011. The device is manufactured by HEYER MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is FOR ANY MEDICAL 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 : C
HEYER Vaporizer
Analysis ID: AKL 20403121011

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

FOR ANY MEDICAL INDONESIA

AR Address

Jalan RS Fatmawati (Fatmawati Grand Centre) Blok II Kavling Nomor 215 RT.003 RW.010

Registration Date

May 07, 2024

Expiry Date

Nov 28, 2028

Product Type

Therapeutic Anesthesia Equipment

Anesthetic vaporizer.

Non Electromedic Non Sterile

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