ONEHEALTH SAYONARA FEVER - Indonesia BPOM Medical Device Registration
ONEHEALTH SAYONARA FEVER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11403420178. The device is manufactured by JINHUA JINGDI MEDICAL SUPPLIES CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDICAL ERA ALKESINDO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
JINHUA JINGDI MEDICAL SUPPLIES CO., LTD.Country of Origin
China
Authorized Representative
PT. MEDICAL ERA ALKESINDOAR Address
Jl. Sisingamangaraja Kilometer 10.8, Komplek Amplas Trade Centre Blok Mahoni nomor 08, Kota Medan, Provinsi Sumatera Utara, Kode Pos: 20148
Registration Date
May 17, 2024
Expiry Date
Mar 15, 2027
Product Type
Therapeutic Physical Health Equipment
Cold pack.
Non Electromedic Non Sterile
LIFERESOURCES Microporous Tape
LIFERESOURCES Cooling Gel Sheet
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HEALTHCARE Adhesive Wound Dressing
XPRESFIX Wound Dressing Tape Roll
XPRESPLAST Elastic Plaster Roll
ONEHEALTH Hypo-Pore Paper Surgical Tape With Dispenser
ONEHEALTH Dermaplast Ultra Adhesive Tape
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