KES Intens Pulse Light System - Indonesia BPOM Medical Device Registration
KES Intens Pulse Light System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603718479. The device is manufactured by BEIJING KES BIOLOGY TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BCS PRIMA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BEIJING KES BIOLOGY TECHNOLOGY CO., LTDCountry of Origin
China
Authorized Representative
PT. BCS PRIMA INDONESIAAR Address
Jl. Pondok Kopi Raya Blok A No. 8 RT 009 RW 010
Registration Date
Aug 24, 2021
Expiry Date
Aug 02, 2026
Product Type
Surgical Equipment
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