Pure Global

BD SurePath™ Collection Vial Kit - Indonesia BPOM Medical Device Registration

BD SurePath™ Collection Vial Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20304420081. The device is manufactured by BECTON, DICKINSON AND COMPANY from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
BD SurePath™ Collection Vial Kit
Analysis ID: AKL 20304420081

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

BECTON DICKINSON INDONESIA

AR Address

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

Registration Date

Sep 09, 2024

Expiry Date

Dec 21, 2028

Product Type

Immunology Laboratory Equipment and Reagents

Complement reagent.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing