SHENDA Laparoscope - Indonesia BPOM Medical Device Registration
SHENDA Laparoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801520021. The device is manufactured by SHENYANG SHENDA ENDOSCOPE CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is EDISON AMBASSADOR MEANS.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHENYANG SHENDA ENDOSCOPE CO., LTDCountry of Origin
China
Authorized Representative
EDISON AMBASSADOR MEANSAR Address
Jl. Oasis Sememi Raya No. 1 RT 05 RW 04, Kel. Sememi, Kec. Benowo, Surabaya, Jawa Timur
Registration Date
Jan 15, 2025
Expiry Date
Nov 12, 2029
Product Type
Diagnostic Gastroenterology-Urology Equipment
Endoscope and accessories
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