GIDCARE Lancing Device - Indonesia BPOM Medical Device Registration
GIDCARE Lancing Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603816757. 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 GIDION JAYA.
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Risk Classification
Product Class
Kelas : 1
Country of Origin
China
Authorized Representative
GIDION JAYAAR Address
JL SULTAN HASANUDIN RT 005 / RW 05, AMBON 97128, MALUKU
Registration Date
May 07, 2021
Expiry Date
Dec 31, 2023
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Non Sterile
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NANTONG HOPE INDUSTRY & TRADE CO., LTD.
GIDCARE Alcohol Prep Pad
WUXI MEDICAL INSTRUMENT FACTORY CO., LTD.