ZIMMER Standard Case - Indonesia BPOM Medical Device Registration
ZIMMER Standard Case is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303915602. The device is manufactured by VIANT AS & O HOLDINGS, LLC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. KALMED SEJAHTERA INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
VIANT AS & O HOLDINGS, LLC.Country of Origin
United States
Authorized Representative
PT. KALMED SEJAHTERA INDONESIAAR Address
Jl. TMII Pintu II No. 2, RT 006 RW 004,
Registration Date
May 20, 2022
Expiry Date
Dec 08, 2026
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
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