Pure Global

FISHER & PAYKEL Nasal Prong - Indonesia BPOM Medical Device Registration

FISHER & PAYKEL Nasal Prong is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403718409. The device is manufactured by FISHER & PAYKEL HEALTHCARE S.A. DE C.V. from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MURSMEDIC.

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
FISHER & PAYKEL Nasal Prong
Analysis ID: AKL 20403718409

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Mexico

Authorized Representative

PT. MURSMEDIC

AR Address

Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat

Registration Date

Nov 10, 2022

Expiry Date

May 19, 2025

Product Type

Therapeutic Anesthesia Equipment

Ventilator tubing.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Similar Products (1)
Other products with the same name
Other Products from FISHER & PAYKEL HEALTHCARE S.A. DE C.V.
Products from the same manufacturer (2 products)