Pure Global

OXOID VORICONAZOLE VOR 10 µg - Indonesia BPOM Medical Device Registration

OXOID VORICONAZOLE VOR 10 µg is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20301700823. The device is manufactured by OXOID LIMITED. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DIPA PUSPA LABSAINS.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
OXOID VORICONAZOLE VOR 10 µg
Analysis ID: AKL 20301700823

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

OXOID LIMITED.

Country of Origin

United Kingdom

Authorized Representative

PT. DIPA PUSPA LABSAINS

AR Address

Dipa Strategic Office, Lantai Lobby, Jl. Raya Kebayoran Lama No.28 RT.009/RW.011, Kel. Grogol Utara, Kec. Kebayoran Lama

Registration Date

Nov 28, 2022

Expiry Date

Sep 26, 2025

Product Type

Diagnostic Equipment

Antimicrobial susceptibility test disc.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing