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ENCOR ULTRA Breast Biopsy System and Accessories - Indonesia BPOM Medical Device Registration

ENCOR ULTRA Breast Biopsy System and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801020817. The device is manufactured by DYMAX, CORP. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRO-HEALTH INTERNATIONAL.

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BPOM Registered
Risk Class Kelas Resiko : B
ENCOR ULTRA Breast Biopsy System and Accessories
Analysis ID: AKL 20801020817

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

DYMAX, CORP.

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

Jun 10, 2022

Expiry Date

Feb 08, 2027

Product Type

Diagnostic Gastroenterology-Urology Equipment

Gastroenterology-urology biopsy instrument

Non Radiation Electromedics

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