NEONA Safety Lancet - Indonesia BPOM Medical Device Registration
NEONA Safety Lancet is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603323952. The device is manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. UBC MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Country of Origin
China
Authorized Representative
PT. UBC MEDICAL INDONESIAAR Address
Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930
Registration Date
May 05, 2023
Expiry Date
Feb 23, 2025
Product Type
Surgical Equipment
Manual surgical instrument for general use
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