ROSA Knee System - Indonesia BPOM Medical Device Registration
ROSA Knee System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21002320143. The device is manufactured by ZIMMER CAS from Canada, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. KALMED SEJAHTERA INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ZIMMER CASCountry of Origin
Canada
Authorized Representative
PT. KALMED SEJAHTERA INDONESIAAR Address
JL.TAMAN MINI PINTU 2 NO. 2, RT. 006 RW. 004
Registration Date
Sep 27, 2024
Expiry Date
Dec 08, 2026
Product Type
Surgical Neurology Equipment
Stereotaxic instrument.
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