GENTLE PRO - Indonesia BPOM Medical Device Registration
GENTLE PRO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805917469. The device is manufactured by ZIMMER MEDIZINSYSTEME GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. I-TECH LAFACOS.
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
ZIMMER MEDIZINSYSTEME GMBHCountry of Origin
Germany
Authorized Representative
PT. I-TECH LAFACOSAR Address
Gedung indra centra Blok M-N, Jl. Jendral suprapto No. 60, Kel Cempaka Putih barat , Kec. Cempaka Putih
Registration Date
Oct 06, 2023
Expiry Date
Jul 25, 2028
Product Type
Therapeutic Gastroenterology-Urology Equipment
Extracorporeal shock wave lithotripter.
Non Radiation Electromedics
DISCOVERY Pico Derm
QUANTA SYSTEM S.P.A.
LITHO DK30
QUANTA SYSTEM S.P.A.
LITHO 100
QUANTA SYSTEM S.P.A
LITHO 150
QUANTA SYSTEM S.P.A
CHROME
QUANTA SYSTEM S.P.A
GUNA MD-KNEE H
USE S.P.A.
RENUVION System Generator
APYX BULGARIA LTD.
BVLASER CO2 Laser Machine
NANJING BESTVIEW LASER S&T CO., LTD.
SYNOLIS VA 80/160
SKIN TECH PHARMA GROUP, S.L
By Wave Med
ZIMMER MEDIZINSYSTEME GMBH