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FISHER & PAYKEL Resuscitation T-Piece Kit - Indonesia BPOM Medical Device Registration

FISHER & PAYKEL Resuscitation T-Piece Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403812129. 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. 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.

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BPOM Registered
Risk Class Kelas Resiko : B
FISHER & PAYKEL Resuscitation T-Piece Kit
Analysis ID: AKL 20403812129

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

New Zealand

Authorized Representative

PT. MURSMEDIC

AR Address

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

Registration Date

Sep 23, 2022

Expiry Date

May 19, 2025

Product Type

Therapeutic Anesthesia Equipment

Manual emergency ventilator.

Non Electromedic Non Sterile

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