DUO FULL HD S195 - Indonesia BPOM Medical Device Registration
DUO FULL HD S195 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801021677. The device is manufactured by PUFF from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is VERSACON MEDICAL.
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
PUFFCountry of Origin
France
Authorized Representative
VERSACON MEDICALAR Address
JL ANGGREK NELI MURNI BLOK C NO 30-30 A, PALMERAH
Registration Date
Mar 31, 2020
Expiry Date
Mar 25, 2024
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories
Non Radiation Electromedics
NOVALITH NT30 Intracorporeal Pneumatic Lithotripter
NOVAMEDTEK MEDIKAL VE TIBBI CIHAZLAR SAN. VE TIC LTD., STI.
CUSAยฎย Clarity Sterilization Tray
INTEGRA LIFESCIENCES (IRELAND) LIMITED
ACKERMANN Instrument Nephroscopy Set
ACKERMANN INSTRUMENTE GMBH
ACKERMANN - INSTRUMENT URETHROTOMY SET
ACKERMANN INSTRUMENTE GMBH
POLYDIAGNOST - Endoscopic Instrument Set and accessories
POLYDIAGNOST GMBH
BLOW 165 DUO
PUFF

