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BD SurePath™ Direct to Slide Kit - Indonesia BPOM Medical Device Registration

BD SurePath™ Direct to Slide Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20201420147. 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.

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BPOM Registered
Risk Class Kelas Resiko : B
BD SurePath™ Direct to Slide Kit
Analysis ID: AKL 20201420147

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 24, 2024

Expiry Date

Dec 21, 2028

Product Type

Biological Dyes

Cervical intraepithelial neoplasia (CIN) test system

Invitro Diagnostics

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