RUSCH - SUPERGLIDE DD Tumour Ureter Stent Set - Indonesia BPOM Medical Device Registration
RUSCH - SUPERGLIDE DD Tumour Ureter Stent Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804814231. The device is manufactured by ARROW INTERNATIONAL CR A.S. from Czech Republic, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. LABORA MANDIRI INDO PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ARROW INTERNATIONAL CR A.S.Country of Origin
Czech Republic
Authorized Representative
PT. LABORA MANDIRI INDO PRATAMAAR Address
Jl. C. Simanjuntak No. 47, RT.014, RW.003, Desa/Kelurahan Terban, Kecamanan Gondokusuman, Kota Yogyakarta, Provinsi Daerah Istimewa Yogyakarta, Kode Pos : 55223
Registration Date
Nov 14, 2023
Expiry Date
Dec 31, 2025
Product Type
Gastroenterology-Surgical Urology Equipment
Ureteral stent.
Non Electromedic Sterile
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