POWERSEAL - Indonesia BPOM Medical Device Registration
POWERSEAL is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603325028. The device is manufactured by GYRUS ACMI, INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MURSMEDIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GYRUS ACMI, INC.Country of Origin
United States
Authorized Representative
MURSMEDICAR Address
Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat
Registration Date
Sep 18, 2023
Expiry Date
Mar 31, 2026
Product Type
Surgical Equipment
Electrosurgical cutting and coagulation device and accessories.
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