JIZHEN YFY-KN95 Class FFP-2 - Indonesia BPOM Medical Device Registration
JIZHEN YFY-KN95 Class FFP-2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903026850. The device is manufactured by JIANGXI YIFENGYUAN BIOLOGICAL ENGINEERING CO. LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SONNA MEDIKA JAYA.
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
Country of Origin
China
Authorized Representative
PT. SONNA MEDIKA JAYAAR Address
Rukan Sentra Niaga Blok M, Green Lake City, No.017 RT. 007 RW.008, Duri Kosambi, Cengkareng, Jakarta Barat
Registration Date
Nov 10, 2020
Expiry Date
Sep 20, 2025
Product Type
General Hospital Equipment and Other Individuals
Filtering facepiece respirator for use by the general public in public health medical emergencies.
Non Electromedic Non Sterile
LensHooke Sperm DNA Fragmentation Rapid Test Kit (SCD Assay)
BONRAYBIO CO., LTD.
CRYOTOP SAFETY KIT
KITAZATO CORPORATION
CRYOTOP SAFETY KIT
KITAZATO CORPORATION
WISONIC NAVI Color Doppler Ultrasound
SHENZHEN WISONIC MEDICAL TECHNOLOGY CO., LTD.
WISONIC Ultrasonic Diagnostic System
SHENZHEN WISONIC MEDICAL TECHNOLOGY CO., LTD.
WISONIC Ultrasonic Diagnostic System
SHENZHEN WISONIC MEDICAL TECHNOLOGY CO., LTD.
C3 CryoSystem
INOMED MEDIZINTECHNIK GMBH
PROSONNA Diagnostic Ultrasound System
SONOSCAPE MEDICAL CORP.
WISONIC Ultrasonic Diagnostic System
SHENZHEN WISONIC MEDICAL TECHNOLOGY CO., LTD
WISONIC Ultrasonic Diagnostic System
SHENZHEN WISONIC MEDICAL TECHNOLOGY CO., LTD.