PANTERA Pro Coronary Dilatation Catheter - Indonesia BPOM Medical Device Registration
PANTERA Pro Coronary Dilatation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505420099. The device is manufactured by BIOTRONIK AG from Switzerland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. DCH AURIGA INDONESIA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
BIOTRONIK AGCountry of Origin
Switzerland
Authorized Representative
PT. DCH AURIGA INDONESIAAR Address
DCH AURIGA INDONESIA
Registration Date
Aug 05, 2024
Expiry Date
May 04, 2028
Product Type
Therapeutic Cardiology Equipment
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