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TERRAGENE BIONOVA Biological Indicator - Indonesia BPOM Medical Device Registration

TERRAGENE BIONOVA Biological Indicator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20901320580. The device is manufactured by TERRAGENE S.A. from Argentina, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.

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BPOM Registered
Risk Class Kelas Resiko : B
TERRAGENE BIONOVA Biological Indicator
Analysis ID: AKL 20901320580

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

TERRAGENE S.A.

Country of Origin

Argentina

Authorized Representative

PT. SURGIKA ALKESINDO

AR Address

Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih

Registration Date

Aug 22, 2023

Expiry Date

Jun 06, 2024

Product Type

General and Individual Hospital Equipment Monitoring

Sterilization process indicator.

Non Electromedic Non Sterile

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