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SYNTHES Femoral Neck System - Indonesia BPOM Medical Device Registration

SYNTHES Femoral Neck System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302320640. The device is manufactured by SYNTHES GMBH from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is JOHNSON AND JOHNSON INDONESIA TWO.

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BPOM Registered
Risk Class Kelas Resiko : C
SYNTHES Femoral Neck System
Analysis ID: AKL 21302320640

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

SYNTHES GMBH

Country of Origin

Switzerland

Authorized Representative

JOHNSON AND JOHNSON INDONESIA TWO

AR Address

K-Link Tower, Lt. 15, Jl. Jend. Gatot Subroto kav. 59A, Kuningan, Setiabudi, Jakarta Selatan, Desa/Kelurahan Kuningan Timur, Kec. Setiabudi, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos: 12950

Registration Date

Apr 25, 2023

Expiry Date

Nov 29, 2027

Product Type

Prosthetic Orthopedic Equipment

Single/multiple component metallic bone fixation appliances and accessories.

Non Electromedic Sterile

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