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SYNCHROMED II Infusion Pump - Indonesia BPOM Medical Device Registration

SYNCHROMED II Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30902812971. The device is manufactured by MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : D
SYNCHROMED II Infusion Pump
Analysis ID: AKL 30902812971

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

United States

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda, Desa/Kelurahan Kebayoran Lama Utara, Kec. Kebayoran Lama

Registration Date

Dec 04, 2023

Expiry Date

Feb 07, 2028

Product Type

Therapeutic General and Individual Hospital Equipment

Implanted programmable infusion pump

Non Electromedic Sterile

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