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BD VENFLON ™ Pro IV Cannula - Indonesia BPOM Medical Device Registration

BD VENFLON ™ Pro IV Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220132. The device is manufactured by BECTON DICKINSON INDIA PVT. LTD. from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. BECTON DICKINSON INDONESIA.

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
BD VENFLON ™ Pro IV Cannula
Analysis ID: AKL 20902220132

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. BECTON DICKINSON INDONESIA

AR Address

Sampoerna Strategic Square South Tower 20th Floor Jl. Jend. Sudirman Kav 45-46

Registration Date

Aug 22, 2024

Expiry Date

Apr 07, 2026

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular catheter.

Non Electromedic Sterile

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