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BIOPINCE Full Core Biopsy Instrument - Indonesia BPOM Medical Device Registration

BIOPINCE Full Core Biopsy Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801516350. The device is manufactured by ARGON MEDICAL DEVICES INC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DIAN LANGGENG PRATAMA.

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BPOM Registered
Risk Class Kelas Resiko : C
BIOPINCE Full Core Biopsy Instrument
Analysis ID: AKL 20801516350

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. DIAN LANGGENG PRATAMA

AR Address

Jl. Raden Saleh Raya No. 4

Registration Date

Aug 27, 2021

Expiry Date

Jan 22, 2025

Product Type

Diagnostic Gastroenterology-Urology Equipment

Gastroenterology-urology biopsy instrument (electric)

Non Electromedic Sterile

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