TRILOC™ II - Indonesia BPOM Medical Device Registration
TRILOC™ II is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302110702. The device is manufactured by DEPUY INTERNATIONAL LTD from United Kingdom, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is JOHNSON & JOHNSON NEW ZEALAND.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
DEPUY INTERNATIONAL LTDCountry of Origin
United Kingdom
Authorized Representative
JOHNSON & JOHNSON NEW ZEALANDAR Address
K-Link Tower Lt. 12, Jln. Jend. Gatot Subroto Kav. 59 A
Registration Date
Sep 22, 2021
Expiry Date
Aug 09, 2026
Product Type
Prosthetic Orthopedic Equipment
Hip joint metal/polymer constrained cemented or uncemented prosthesis.
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