SUPERGLISS Bipolar Forceps - Indonesia BPOM Medical Device Registration
SUPERGLISS Bipolar Forceps is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603815885. The device is manufactured by SUTTER MEDIZINTECHNIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SUTTER MEDIZINTECHNIK GMBHCountry of Origin
Germany
Authorized Representative
PT. SURGIKA ALKESINDOAR Address
Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih
Registration Date
Aug 03, 2021
Expiry Date
Jan 31, 2024
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
Non Electromedic Non Sterile
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