RUNQIANG Disposable anesthesia needle II - Indonesia BPOM Medical Device Registration
RUNQIANG Disposable anesthesia needle II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403520143. 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 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
ALPHA PRIMERA INDOAR Address
Komplek Ruko Taman Meruya Plaza Blok E14 No. 3A, Lt 1
Registration Date
Feb 12, 2025
Expiry Date
May 05, 2029
Product Type
Therapeutic Anesthesia Equipment
Anesthesia conduction needle.
Non Electromedic Sterile
