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MEDTRONIC Spinal Needle - Indonesia BPOM Medical Device Registration

MEDTRONIC Spinal Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403818458. The device is manufactured by MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
MEDTRONIC Spinal Needle
Analysis ID: AKL 20403818458

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

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

Oct 05, 2020

Expiry Date

Mar 11, 2025

Product Type

Therapeutic Anesthesia Equipment

Anesthesia conduction needle.

Non Electromedic Sterile

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