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WEM Argon Plasma Coagulator - Indonesia BPOM Medical Device Registration

WEM Argon Plasma Coagulator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603712588. The device is manufactured by WEM ELECTRONIC EQUIPMENT LTDA. from Brazil, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MEDTRONIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
WEM Argon Plasma Coagulator
Analysis ID: AKL 21603712588

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Brazil

Authorized Representative

MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda, Desa/Kelurahan Kebayoran Lama Utara, Kec. Kebayoran Lama

Registration Date

Nov 01, 2024

Expiry Date

Feb 20, 2029

Product Type

Surgical Equipment

Electrosurgical cutting and coagulation device and accessories.

Non Radiation Electromedics

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