GOBBLE Percussion Reflex Hammer - Indonesia BPOM Medical Device Registration
GOBBLE Percussion Reflex Hammer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11001126639. The device is manufactured by GOBBLE SURGICAL INC. from Pakistan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PUTRASEJATI BUSINESS SUCCESS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
GOBBLE SURGICAL INC.Country of Origin
Pakistan
Authorized Representative
PUTRASEJATI BUSINESS SUCCESSAR Address
Rukan Crown Blok A No.35 Green Lake City, Kel.Petir Kec.Cipondoh, Kota Tangerang 15147
Registration Date
Nov 06, 2021
Expiry Date
Jul 18, 2024
Product Type
Diagnostic Neurology Equipment
Percussor.
Non Electromedic Non Sterile

