MIXI Bags 1000P - Indonesia BPOM Medical Device Registration
MIXI Bags 1000P is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902022522. The device is manufactured by HEGEWALD MEDIZINPRODUKTE GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MULTI RAY ADAMAR.
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
HEGEWALD MEDIZINPRODUKTE GMBHCountry of Origin
Germany
Authorized Representative
PT. MULTI RAY ADAMARAR Address
Ruko Gading Bukit Indah Jl. Bukit Gading Raya L-27 Kelapa Gading, Jakarta Utara
Registration Date
Apr 19, 2023
Expiry Date
Dec 31, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
I.V. container.
Non Electromedic Sterile
