LANTEX Single Use Intraluminal Circular Stapler - Indonesia BPOM Medical Device Registration
LANTEX Single Use Intraluminal Circular Stapler is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603221361. The device is manufactured by SUZHOU LANTEX MEDICAL TECHNOLOGY, CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN MEDICAL SYNERGY.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SUZHOU LANTEX MEDICAL TECHNOLOGY, CO., LTDCountry of Origin
China
Authorized Representative
PT. MAIN MEDICAL SYNERGYAR Address
Komplek Taman Palem Lestari Blok P No. 3 Lantai 3
Registration Date
Jun 07, 2022
Expiry Date
Apr 06, 2025
Product Type
Surgical Equipment
Implantable staple.
Non Electromedic Sterile
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