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FOCUS Implant Set - Indonesia BPOM Medical Device Registration

FOCUS Implant Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11103127797. The device is manufactured by CEATEC MEDIZINTECHNIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FOCUS DIAGNOSTIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : A
FOCUS Implant Set

FOKUS Implant Set

Analysis ID: AKL 11103127797

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. FOCUS DIAGNOSTIC INDONESIA

AR Address

Jl. Jatipadang Raya No.9A, RT.6/RW.4, Kelurahan Jatipadang, Kecamatan Pasar Minggu, Kota Jakarta Selatan, DKI Jakarta 12540

Registration Date

Sep 11, 2024

Expiry Date

Mar 07, 2027

Product Type

Surgical Obstetric and Gynaecological Equipment

Obstetric-gynecologic general manual instrument.

Non Electromedic Non Sterile

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