FOOTPRINT PK Suture Anchor - Indonesia BPOM Medical Device Registration
FOOTPRINT PK Suture Anchor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302313311. The device is manufactured by SMITH & NEPHEW INC., ENDOSCOPY DIVISION from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SMITH & NEPHEW INC., ENDOSCOPY DIVISIONCountry of Origin
United States
Authorized Representative
PT. TAWADA HEALTHCAREAR Address
Rukan Permata Senayan Blok A18-19 Lantai 1-2 Jl. Tentara Pelajar No. 5
Registration Date
Jan 24, 2022
Expiry Date
Dec 31, 2024
Product Type
Prosthetic Orthopedic Equipment
Smooth or threaded metallic bone fixation fastener.
Non Electromedic Sterile
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