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OPTIVA 2 I.V Catheter Radiopaque Polyurethane - Indonesia BPOM Medical Device Registration

OPTIVA 2 I.V Catheter Radiopaque Polyurethane is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902805068. The device is manufactured by SMITHS MEDICAL ITALIA S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. RAJAWALI NUSINDO.

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 : C
OPTIVA 2 I.V Catheter Radiopaque Polyurethane
Analysis ID: AKL 20902805068

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

PT. RAJAWALI NUSINDO

AR Address

Gedung RNI Jl. Denpasar Raya Kav DIII Kuningan Jakarta Selatan

Registration Date

Oct 19, 2023

Expiry Date

Sep 18, 2028

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular catheter.

Non Electromedic Sterile

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