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SYNTHES Forceps System - Indonesia BPOM Medical Device Registration

SYNTHES Forceps System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303320465. The device is manufactured by SYNTHES GMBH from Switzerland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. JOHNSON AND JOHNSON INDONESIA TWO.

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BPOM Registered
Risk Class Kelas Resiko : A
SYNTHES Forceps System
Analysis ID: AKL 11303320465

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

SYNTHES GMBH

Country of Origin

Switzerland

Authorized Representative

PT. 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

Jul 31, 2023

Expiry Date

Nov 29, 2027

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Non Sterile

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