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ACUTRAK 2 Headless Compression System Instruments - Indonesia BPOM Medical Device Registration

ACUTRAK 2 Headless Compression System Instruments is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303220246. The device is manufactured by ACUMED LLC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PRO-HEALTH INTERNATIONAL.

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BPOM Registered
Risk Class Kelas Resiko : A
ACUTRAK 2 Headless Compression System Instruments
Analysis ID: AKL 11303220246

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

ACUMED LLC.

Country of Origin

United States

Authorized Representative

PT. PRO-HEALTH INTERNATIONAL

AR Address

Komplek Perkantoran Duta Merlin Blok C 35-36 Jalan Gajah Mada 3-5

Registration Date

Oct 08, 2022

Expiry Date

Jan 12, 2027

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Non Sterile

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