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MEDTRONIC SEXTANT II Reusable Instrument - Indonesia BPOM Medical Device Registration

MEDTRONIC SEXTANT II Reusable Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303023485. The device is manufactured by MEDTRONIC SOFAMOR DANEK USA, INC from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : A
MEDTRONIC SEXTANT II Reusable Instrument
Analysis ID: AKL 11303023485

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

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

Oct 31, 2024

Expiry Date

Feb 19, 2029

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Non Sterile

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