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INTERSTIM Quadripolar Lead for Electrical Stimulation - Indonesia BPOM Medical Device Registration

INTERSTIM Quadripolar Lead for Electrical Stimulation is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30805810130. The device is manufactured by MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA 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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Risk Class Kelas Resiko : D
INTERSTIM Quadripolar Lead for Electrical Stimulation
Analysis ID: AKL 30805810130

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

Aug 16, 2020

Expiry Date

Mar 12, 2025

Product Type

Therapeutic Gastroenterology-Urology Equipment

Implanted electrical urinary continence device.

Non Electromedic Sterile

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