ANSPACH XMAX Handpiece System - Indonesia BPOM Medical Device Registration
ANSPACH XMAX Handpiece System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21002916293. The device is manufactured by ANSPACH EFFORT, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. JOHNSON & JOHNSON NEW ZEALAND.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ANSPACH EFFORT, INC.Country of Origin
United States
Authorized Representative
PT. JOHNSON & JOHNSON NEW ZEALANDAR Address
K-Link Tower Lt. 12, Jln. Jend. Gatot Subroto Kav. 59 A
Registration Date
Oct 07, 2019
Expiry Date
Jun 04, 2024
Product Type
Surgical Neurology Equipment
Pneumatic cranial drill motor.
Non Electromedic Non Sterile
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