HICO Aquatherm 660 - Indonesia BPOM Medical Device Registration
HICO Aquatherm 660 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20505220074. The device is manufactured by PFM MEDICAL HICO GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is GRAHA ISMAYA.
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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
PFM MEDICAL HICO GMBHCountry of Origin
Germany
Authorized Representative
GRAHA ISMAYAAR Address
Jalan Sultan Iskandar Muda Kav. 24 Arteri Pondok Indah
Registration Date
Nov 08, 2023
Expiry Date
Dec 31, 2026
Product Type
Therapeutic Cardiology Equipment
Thermal regulating system.
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