BLOW 617 - Indonesia BPOM Medical Device Registration
BLOW 617 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20603320587. The device is manufactured by PUFF from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DENTALITIES GROUP ASIA.
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.
SOPRO 617
Risk Classification
Product Class
Kelas : 2
Manufacturer
PUFFCountry of Origin
France
Authorized Representative
PT. DENTALITIES GROUP ASIAAR Address
Graha Samastya Jl. Alaydrus No. 27 D RT 017 RW 003
Registration Date
May 12, 2023
Expiry Date
Dec 02, 2027
Product Type
Surgical Dental Equipment
Dental handpiece and accessories
Non Radiation Electromedics
HAISHU Dental Unit
NINGBO HAISHU ESCO MEDICAL TECHNOLOGY CO., LTD.
EURONDA Monoart Saliva Ejectors
EURONDA S.P.A,
MICO ONE Orthodontic Screw
ZE FANG TECHNOLOGY CO., LTD.
SATELEC NEWTRON P5 XS B.LED
SATELEC
SERVOTOME RANGE II 23OV CE
SATELEC, A COMPANY OF ACTEON GROUP
SATELEC PIEZOTOME CUBE EMB CEE
SATELEC
SEMORR Dental Microscope
SUZHOU SEMORR MEDICAL TECHNOLOGY CO., LTD.
BOMEDENT eHeater (Endodontic Obturation Devices)
CHANGZHOU BOMEDENT MEDICAL TECHNOLOGY, CO.,LTD
BOMEDENT iRoot apex (Apex Locators)
CHANGZHOU BOMEDENT MEDICAL TECHNOLOGY, CO.,LTD
BOMEDENT iRoot Pro
CHANGZHOU BOMEDENT MEDICAL TECHNOLOGY, CO.,LTD