PRO-MAG Ultra Automatic Biopsy Instrument - Indonesia BPOM Medical Device Registration
PRO-MAG Ultra Automatic Biopsy Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801515219. The device is manufactured by ARGON MEDICAL DEVICES INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DIAN LANGGENG PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ARGON MEDICAL DEVICES INC.Country of Origin
United States
Authorized Representative
PT. DIAN LANGGENG PRATAMAAR Address
Gedung Dinar, Jl. Raden Saleh Raya No. 4 RT.10/RW.01, Kel. Kenari, Kec. Senen. Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta, Kode Pos 10430
Registration Date
Jul 29, 2024
Expiry Date
Feb 05, 2029
Product Type
Diagnostic Gastroenterology-Urology Equipment
Gastroenterology-urology biopsy instrument
Non Electromedic Non Sterile
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