NESCO Lanze Lancing Device - Indonesia BPOM Medical Device Registration
NESCO Lanze Lancing Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603811349. The device is manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DJUNIAR & DJUNIAR.
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Risk Classification
Product Class
Kelas : 1
Country of Origin
China
Authorized Representative
PT. DJUNIAR & DJUNIARAR Address
KOMPLEK RUKAN MAHKOTA ANCOL BLOK D NO. 26
Registration Date
Feb 26, 2021
Expiry Date
Dec 31, 2023
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Sterile
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