BOWA Lotus LG4 - Indonesia BPOM Medical Device Registration
BOWA Lotus LG4 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603818732. The device is manufactured by SRA DEVELOPMENT LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ESA MEDIKA MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SRA DEVELOPMENT LTD.Country of Origin
United Kingdom
Authorized Representative
PT. ESA MEDIKA MANDIRIAR Address
ESA 8 Building, 10th Floor, Jl. Ir. Soekarno Kavling 3-5
Registration Date
Sep 25, 2021
Expiry Date
Dec 31, 2025
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
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