STERIMAR BLOCKED Nose Baby - Indonesia BPOM Medical Device Registration
STERIMAR BLOCKED Nose Baby is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20704025218. The device is manufactured by CHURCH & DWIGHT UK LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. KEBAYORAN PHARMA.
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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
CHURCH & DWIGHT UK LTD.Country of Origin
United Kingdom
Authorized Representative
PT. KEBAYORAN PHARMAAR Address
Jl. Garuda No.79 Jakarta Pusat, 10610
Registration Date
Apr 05, 2022
Expiry Date
Mar 07, 2027
Product Type
Therapeutic Ear, Nose and Throat Equipment
Nasal irrigation solution
Non Electromedic Non Sterile
HYLACELL Hydrogel Wound Dressing
INCORE CO., LTD.
ENTCLEAR
SHIH-KANG MEDICAL INSTRUMENTS CO., LTD.
STERIMAR NOSE PRONE TO COLDS
CHURCH & DWIGHT UK LTD.
STERIMAR Nose Hygiene and Comfort
CHURCH & DWIGHT UK LTD.
STERIMAR Blocked Nose
CHURCH & DWIGHT UK LTD.
STERIMAR Baby Nose Hygiene
CHURCH & DWIGHT UK LTD.

