FAMILY Dr. ™ AKTIVESAFE Lancet - Indonesia BPOM Medical Device Registration
FAMILY Dr. ™ AKTIVESAFE Lancet is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603027298. The device is manufactured by BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. INDOCORE PERKASA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
BEIJING RUICHENG MEDICAL SUPPLIES CO., LTD.Country of Origin
China
Authorized Representative
PT. INDOCORE PERKASAAR Address
Komplek Graha Mas Pemuda Blok AB No. 19, Jl. Pemuda RT 020 / RW 006
Registration Date
Jul 11, 2024
Expiry Date
Aug 05, 2025
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Sterile
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