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ACROSS CTO PTCA Dilatation Catheter - Indonesia BPOM Medical Device Registration

ACROSS CTO PTCA Dilatation Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501810699. The device is manufactured by ACROSTAK (SCHWEIZ) AG. from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HARMONI PRIMA MEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : C
ACROSS CTO PTCA Dilatation Catheter
Analysis ID: AKL 20501810699

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Switzerland

Authorized Representative

PT. HARMONI PRIMA MEDIKA

AR Address

Jl. Tanjung Selor No. 1A, Cideng, Gambir, Jakarta Pusat, 10150

Registration Date

Dec 29, 2021

Expiry Date

Aug 28, 2026

Product Type

Therapeutic Cardiology Equipment

Percutaneous Transluminal Coronary Angioplasty (PTCA) Catheter

Non Electromedic Sterile

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