RUNQIANG Anesthesia Epidural Catheter - Indonesia BPOM Medical Device Registration
RUNQIANG Anesthesia Epidural Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420765. The device is manufactured by ZHEJIANG RUNQIANG MEDICAL INSTRUMENTS CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ALPHA PRIMERA INDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ZHEJIANG RUNQIANG MEDICAL INSTRUMENTS CO., LTDCountry of Origin
China
Authorized Representative
PT. ALPHA PRIMERA INDOAR Address
Komplek Ruko Taman Meruya Plaza Blok E14 No. 3A, Lt 1
Registration Date
Feb 10, 2025
Expiry Date
Sep 04, 2029
Product Type
Therapeutic Anesthesia Equipment
Anesthesia conduction catheter.
Non Electromedic Sterile
