JB MED Endoscopic Gastrostomy (PEG) KIT - Indonesia BPOM Medical Device Registration
JB MED Endoscopic Gastrostomy (PEG) KIT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420122. The device is manufactured by BEIJING ZKSK TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MAIN ONCOPROBE.
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
BEIJING ZKSK TECHNOLOGY CO., LTDCountry of Origin
China
Authorized Representative
PT. MAIN ONCOPROBEAR Address
APRT.ISTANA HARMONI LT.DASAR UNIT 1M, KOMP.HARMONI PLAZA JL.SURYOPRANOTO NO.2, PETOJO UTARA
Registration Date
Feb 27, 2024
Expiry Date
Feb 26, 2027
Product Type
Therapeutic Gastroenterology-Urology Equipment
Gastrointestinal tube and accessories.
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