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PercuTrach® dilatation set I - Indonesia BPOM Medical Device Registration

PercuTrach® dilatation set I is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403020227. The device is manufactured by PRIMED HALBERSTADT MEDIZINTECHNIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOPRIMA BIONET.

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BPOM Registered
Risk Class Kelas Resiko : B
PercuTrach® dilatation set I
Analysis ID: AKL 20403020227

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. INDOPRIMA BIONET

AR Address

Jalan Tamansari Raya, Komplek 56 No. 56 B Jakarta Barat 11150

Registration Date

Dec 08, 2022

Expiry Date

Dec 31, 2026

Product Type

Therapeutic Anesthesia Equipment

Tracheostomy tube and tube cuff.

Non Electromedic Sterile

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