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ASCENDA INTRATHECAL CATHETER 8780 SPINAL SEGMENT - Indonesia BPOM Medical Device Registration

ASCENDA INTRATHECAL CATHETER 8780 SPINAL SEGMENT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31002817002. 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
ASCENDA INTRATHECAL CATHETER 8780 SPINAL SEGMENT
Analysis ID: AKL 31002817002

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

Registration Date

Sep 06, 2020

Expiry Date

Mar 12, 2025

Product Type

Surgical Neurology Equipment

Intratechal catheter

Non Electromedic Sterile

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