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PIONEER Plus Catheter - Indonesia BPOM Medical Device Registration

PIONEER Plus Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501810432. The device is manufactured by VIANT AS & O HOLDINGS, LLC. from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRANSMEDIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
PIONEER Plus Catheter
Analysis ID: AKL 20501810432

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. TRANSMEDIC INDONESIA

AR Address

PERKANTORAN MENARA ERA UNIT G-01, JL. SENEN RAYA NO. 135-137

Registration Date

Nov 17, 2020

Expiry Date

Sep 23, 2024

Product Type

Diagnostic Cardiology Equipment

Percutaneous catheter.

Non Electromedic Sterile

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