APT Transseptal Needle and Sheath - Indonesia BPOM Medical Device Registration
APT Transseptal Needle and Sheath is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501711500. The device is manufactured by APT MEDICAL INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GIRI SAKTI UTAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
APT MEDICAL INC.Country of Origin
China
Authorized Representative
PT. GIRI SAKTI UTAMAAR Address
Komp. Girimekar Permai Blok D No. 15 RT. 03 RW. 21 Desa Giri Mekar Kec. Cilengkrang
Registration Date
Nov 17, 2021
Expiry Date
Oct 21, 2026
Product Type
Diagnostic Cardiology Equipment
Catheter introducer.
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