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ASCENDA Intrathecal Catheter with an 66 cm Spinal Segment - Indonesia BPOM Medical Device Registration

ASCENDA Intrathecal Catheter with an 66 cm Spinal Segment is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31002816893. 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 with an 66 cm Spinal Segment
Analysis ID: AKL 31002816893

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, Desa/Kelurahan Kebayoran Lama Utara, Kec. Kebayoran Lama

Registration Date

Nov 24, 2023

Expiry Date

Feb 06, 2028

Product Type

Surgical Neurology Equipment

Intratechal catheter

Non Electromedic Sterile

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