HUGEMED Single-use RhinoLaryngoscope - Indonesia BPOM Medical Device Registration
HUGEMED Single-use RhinoLaryngoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420252. The device is manufactured by SHENZHEN HUGEMED MEDICAL TECHNICAL DEVELOPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. EUPHRATES WITH.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. EUPHRATES WITHAR Address
Ruko Gardenia kav 1, jln. parigi raya no 75 sukabakti curug 15810
Registration Date
Jun 19, 2024
Expiry Date
Nov 29, 2028
Product Type
Therapeutic Anesthesia Equipment
Flexible laryngoscope.
Non Radiation Electromedics
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