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VALLEYLAB™ Tungsten Loop Electrodes - Indonesia BPOM Medical Device Registration

VALLEYLAB™ Tungsten Loop Electrodes is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603713797. The device is manufactured by BOVIE MEDICAL CORPORATION from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
VALLEYLAB™ Tungsten Loop Electrodes
Analysis ID: AKL 21603713797

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda

Registration Date

Dec 30, 2020

Expiry Date

Mar 12, 2025

Product Type

Surgical Equipment

Electrosurgical cutting and coagulation device and accessories.

Non Electromedic Sterile

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