Pure Global

BLUE CROSS Silicone Resuscitator Adult - Indonesia BPOM Medical Device Registration

BLUE CROSS Silicone Resuscitator Adult is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403513047. The device is manufactured by BLUE CROSS EMERGENCY CO., LTD. KAWAGOE FACTORY from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOBAL JAYA MEDIKA.

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
BLUE CROSS Silicone Resuscitator Adult
Analysis ID: AKL 20403513047

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

PT. GLOBAL JAYA MEDIKA

AR Address

Jl.Penjernihan I No.38 RT 05 RW 06,Gedung Bersaudara Group Lt. 3A Lot.001- 003 & 005.

Registration Date

Mar 20, 2024

Expiry Date

Mar 31, 2027

Product Type

Therapeutic Anesthesia Equipment

Manual emergency ventilator.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from BLUE CROSS EMERGENCY CO., LTD. KAWAGOE FACTORY
Products from the same manufacturer (2 products)