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BD BBL™ Salmonella Shigella Agar - Indonesia BPOM Medical Device Registration

BD BBL™ Salmonella Shigella Agar is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302717592. The device is manufactured by BECTON, DICKINSON AND COMPANY (39L) from United States, and is classified as Risk Class Kelas Resiko : A. 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 : A
BD BBL™ Salmonella Shigella Agar
Analysis ID: AKL 10302717592

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

PT. BECTON DICKINSON INDONESIA

AR Address

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

Registration Date

Jan 20, 2025

Expiry Date

Dec 20, 2028

Product Type

Microbiology Equipment

Selective culture medium.

Invitro Diagnostics

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