P Flex Ureteral Stent & Set - Indonesia BPOM Medical Device Registration
P Flex Ureteral Stent & Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804420112. The device is manufactured by BLUE NEEM MEDICAL DEVICES PRIVATE LIMITED from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BLUE NEEM MEDICAL DEVICES PRIVATE LIMITEDCountry of Origin
India
Authorized Representative
PT. ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
Sep 23, 2024
Expiry Date
Mar 03, 2029
Product Type
Gastroenterology-Surgical Urology Equipment
Ureteral stent.
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PHONAK TERRA+ RIC-312
SONOVA AT
PHONAK TERRA+ BTE-M
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PHONAK TERRA BTE-M
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PHONAK TERRA+ BTE-UP
SONOVA AT