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DENALI Vena Cava Filter - Indonesia BPOM Medical Device Registration

DENALI Vena Cava Filter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30503123493. The device is manufactured by C.R. BARD, INC. from United States, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. ITAMA RANORAYA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : D
DENALI Vena Cava Filter
Analysis ID: AKL 30503123493

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

C.R. BARD, INC.

Country of Origin

United States

Authorized Representative

PT. ITAMA RANORAYA

AR Address

MT Haryono Square Lantai 1 Unit 1, Jl. Otto Iskandardinata Raya No. 390 RT 006 RW 012 Kel. Bidara Cina, Kec. Jatinegara, Jakarta Timur, DKI Jakarta

Registration Date

Nov 08, 2022

Expiry Date

Dec 31, 2025

Product Type

Prosthetic Cardiology Equipment

Cardiovascular intravascular filter.

Non Electromedic Sterile

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