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VIDA I.V.Catheter with Injection - Indonesia BPOM Medical Device Registration

VIDA I.V.Catheter with Injection is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902421006. The device is manufactured by SHANGHAI MEDIC INDUSTRY CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DANVI MEDILAB PERKASA.

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
VIDA I.V.Catheter with Injection
Analysis ID: AKL 20902421006

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DANVI MEDILAB PERKASA

AR Address

Jl. Kapten Muslim Komp. Mega Com Center Blok G No. 1-2 Kel. Dwikora Kec. Medan Helvetia

Registration Date

Sep 12, 2024

Expiry Date

Sep 11, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular catheter.

Non Electromedic Sterile

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