Pure Global

F&P 820 & ACCESSORIES - Indonesia BPOM Medical Device Registration

F&P 820 & ACCESSORIES is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403321658. The device is manufactured by FISHER & PAYKEL HEALTHCARE, LTD from New Zealand, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FISHER AND PAYKEL HEALTHCARE 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
F&P 820 & ACCESSORIES
Analysis ID: AKL 20403321658

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

New Zealand

AR Address

Gandaria 8 Office Tower Lantai 8 Jl. Sultan Iskandar Muda, No.10, RT.10/RW.6. Kec. Kebayoran Lama, Jakarta Selatan 12240, Indonesia.

Registration Date

Oct 02, 2024

Expiry Date

Jun 26, 2028

Product Type

Therapeutic Anesthesia Equipment

Respiratory gas humidifier.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing