LINKFAR Lancing Device - Indonesia BPOM Medical Device Registration
LINKFAR Lancing Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603811994. 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 MACROCITRA ARDANASEJATI.
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Risk Classification
Product Class
Kelas : 1
Country of Origin
China
Authorized Representative
MACROCITRA ARDANASEJATIAR Address
Rukan Taman Meruya Blok M-65 Meruya Ilir - Jakarta Barat Telp. 021-5874575, Fax. 021-5874573
Registration Date
Oct 17, 2022
Expiry Date
Jul 07, 2027
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Sterile
GIDCARE Alcohol Pad
GIDCARE STERILE LANCET FOR SINGLE USE
GIDCARE PEN LANCING DEVICE
LINKFAR Safety Lancets
LIANFA Lancets
LINKFAR Sterile Lancet for Single Use
GIDCARE Lancing Device
GIDCARE Sterile Blood Lancets
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