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HI-TORQUE WHISPER MS Guide Wire - Indonesia BPOM Medical Device Registration

HI-TORQUE WHISPER MS Guide Wire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501611410. The device is manufactured by ABBOTT VASCULAR. from Puerto Rico USA, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ABBOTT PRODUCTS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
HI-TORQUE WHISPER MS Guide Wire
Analysis ID: AKL 20501611410

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

ABBOTT VASCULAR.

Country of Origin

Puerto Rico USA

Authorized Representative

ABBOTT PRODUCTS INDONESIA

AR Address

WISMA PONDOK INDAH 2 SUITE 1000, JL. SULTAN ISKANDAR MUDA KAV. V-TA

Registration Date

Nov 14, 2023

Expiry Date

Mar 14, 2028

Product Type

Diagnostic Cardiology Equipment

Catheter guide wire.

Non Electromedic Sterile

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