LOCOPLEX Regional Analgesia Needle - Indonesia BPOM Medical Device Registration
LOCOPLEX Regional Analgesia Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403321398. The device is manufactured by SIPA from France, 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
SIPACountry of Origin
France
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
Jul 07, 2023
Expiry Date
Dec 31, 2025
Product Type
Therapeutic Anesthesia Equipment
Anesthesia conduction needle.
Non Electromedic Sterile
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