MULTIVERSE Manifold - Indonesia BPOM Medical Device Registration
MULTIVERSE Manifold is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403028335. The device is manufactured by DOLPHIN LIFE SCIENCE INDIA, LLP from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOMED PHARMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DOLPHIN LIFE SCIENCE INDIA, LLPCountry of Origin
India
Authorized Representative
PT. INDOMED PHARMAAR Address
Kelapa Gading Hyper Mall, Lantai Dasar Blok B10 No. 03 (DB1003), Jakarta Utara
Registration Date
Jun 21, 2024
Expiry Date
Aug 14, 2028
Product Type
Therapeutic Anesthesia Equipment
Nonrebreathing valve.
Non Electromedic Sterile
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EXPLORER Angiography Guidewire
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ELIZER Guiding Catheter
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GALACTIC Ballon Inflation Device
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