ENDOVISION UBE Flex Probe - Indonesia BPOM Medical Device Registration
ENDOVISION UBE Flex Probe is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804320305. The device is manufactured by ENDOVISION CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ENDO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ENDOVISION CO., LTD.Country of Origin
Korea
Authorized Representative
ENDO INDONESIAAR Address
Jl. Raya Menganti 14
Registration Date
Feb 26, 2024
Expiry Date
Aug 30, 2026
Product Type
Gastroenterology-Surgical Urology Equipment
Endoscopic electrosurgical unit and accessories.
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