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OPTISTAR MR Syringe - Indonesia BPOM Medical Device Registration

OPTISTAR MR Syringe is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501511975. The device is manufactured by GW PLASTICS, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.

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BPOM Registered
Risk Class Kelas Resiko : B
OPTISTAR MR Syringe
Analysis ID: AKL 20501511975

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

GW PLASTICS, INC.

Country of Origin

United States

Authorized Representative

PT. TAWADA HEALTHCARE

AR Address

Rukan Permata Senayan Blok A18-19 Lantai 1-2 Jl. Tentara Pelajar No. 5

Registration Date

Sep 28, 2020

Expiry Date

Sep 30, 2024

Product Type

Diagnostic Cardiology Equipment

Angiographic injector and syringe.

Non Electromedic Sterile

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