GRIPPER Needle - Indonesia BPOM Medical Device Registration
GRIPPER Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902110850. The device is manufactured by SMITHS HEALTHCARE MANUFACTURING SA DE C.V. from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SMITHS HEALTHCARE MANUFACTURING SA DE C.V.Country of Origin
Mexico
Authorized Representative
PT. IDS MEDICAL SYSTEMS INDONESIAAR Address
Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410
Registration Date
Dec 07, 2020
Expiry Date
Mar 16, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Hypodermic single lumen needle.
Non Electromedic Sterile
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