AK MEDICAL AK- MR Femoral Stem Revision - Indonesia BPOM Medical Device Registration
AK MEDICAL AK- MR Femoral Stem Revision is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302320764. The device is manufactured by BEIJING AK MEDICAL CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PANCA PERSADA 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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
BEIJING AK MEDICAL CO., LTDCountry of Origin
China
Authorized Representative
PANCA PERSADA MEDIKAAR Address
Graha Mampang Lt. 1, Jl. Mampang Prapatan Raya No. 100 RT.002/RW.001, Kel. Duren Tiga, Kec. Pancoran, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos 12760
Registration Date
Jul 09, 2023
Expiry Date
Feb 06, 2028
Product Type
Prosthetic Orthopedic Equipment
Hip joint femoral (hemi-hip) metallic cemented or uncemented prosthesis.
Non Electromedic Sterile
