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VERSAPORT™ Auto Suture™ Bladed Trocar with Fixation Cannula 5mm - Indonesia BPOM Medical Device Registration

VERSAPORT™ Auto Suture™ Bladed Trocar with Fixation Cannula 5mm is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801819224. The device is manufactured by COVIDIEN. from Dominican, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEDTRONIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
VERSAPORT™ Auto Suture™ Bladed Trocar with Fixation Cannula 5mm
Analysis ID: AKL 20801819224

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

COVIDIEN.

Country of Origin

Dominican

Authorized Representative

MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda

Registration Date

Apr 26, 2022

Expiry Date

Feb 16, 2027

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories

Non Electromedic Sterile

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