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BD BACTEC ™ MGIT ™ 960 STR 4.0 Kit - Indonesia BPOM Medical Device Registration

BD BACTEC ™ MGIT ™ 960 STR 4.0 Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20301712902. 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 PT. BECTON DICKINSON INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
BD BACTEC ™ MGIT ™ 960 STR 4.0 Kit
Analysis ID: AKL 20301712902

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. Jend. Sudirman Kav 45-46

Registration Date

Oct 13, 2024

Expiry Date

Dec 21, 2028

Product Type

Diagnostic Equipment

Culture medium for antimicrobial susceptibility tests.

Invitro Diagnostics

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