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BD BBL™ Sensi-Disc™ Aztreonam 30 µg - Indonesia BPOM Medical Device Registration

BD BBL™ Sensi-Disc™ Aztreonam 30 µg is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20301716241. The device is manufactured by BECTON DICKINSON CARIBE LTD. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BECTON DICKINSON INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
BD BBL™ Sensi-Disc™ Aztreonam 30 µg
Analysis ID: AKL 20301716241

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. BECTON DICKINSON INDONESIA

AR Address

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

Registration Date

Dec 17, 2021

Expiry Date

Jun 05, 2025

Product Type

Diagnostic Equipment

Antimicrobial susceptibility test disc.

Invitro Diagnostics

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