PERMEDICA Global Knee System PS - Indonesia BPOM Medical Device Registration
PERMEDICA Global Knee System PS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302321043. The device is manufactured by PERMEDICA S.P.A from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SUNG WON MEDICS GLOBAL.
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
PERMEDICA S.P.ACountry of Origin
Italy
Authorized Representative
PT. SUNG WON MEDICS GLOBALAR Address
RUKO GADING RIVERVIEW BLOK H53, MALL OF INDONESIA, JALAN BOULEVARD BARAT RAYA NOMOR 12
Registration Date
Dec 14, 2023
Expiry Date
Oct 11, 2028
Product Type
Prosthetic Orthopedic Equipment
Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis.
Non Electromedic Sterile
ACS Knee System
IMPLANTCAST GMBH
SUNGWON K-Mixer
DONGGUAN KAISER TECHNOLOGY CO., LTD.
PERMEDICA Hip System
PERMEDICA S.P.A
PERMEDICA Global Knee System RK
PERMEDICA S.P.A
TARIC Total Ankle System
IMPLANTCAST GMBH
AGILON Shoulder System
IMPLANTCAST GMBH
MUTARS Total Knee System
IMPLANTCAST GMBH
BI-FIX Surgical Incision Closure Set
ZHEJIANG HAICHUANG MEDICAL DEVICE CO., LTD.
G21 Bonecement with antibiotic (G1A & G3A)
G21 S.R.L