Pure Global

Flush Nasal and Sinus Wash (Refill) - Indonesia BPOM Medical Device Registration

Flush Nasal and Sinus Wash (Refill) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20704220049. The device is manufactured by GOODY GROUP CO., LTD. from Thailand, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DCH AURIGA 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
Flush Nasal and Sinus Wash (Refill)
Analysis ID: AKL 20704220049

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Thailand

Authorized Representative

DCH AURIGA INDONESIA

AR Address

DCH AURIGA INDONESIA

Registration Date

Dec 26, 2022

Expiry Date

Oct 03, 2027

Product Type

Therapeutic Ear, Nose and Throat Equipment

Nasal irrigation solution

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from GOODY GROUP CO., LTD.
Products from the same manufacturer (2 products)