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MEDICAL SWAN Generator Pulsar - Indonesia BPOM Medical Device Registration

MEDICAL SWAN Generator Pulsar is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603613359. The device is manufactured by ALSA APPARECCHI MEDICALI SRL. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ENDO INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
MEDICAL SWAN Generator Pulsar
Analysis ID: AKL 21603613359

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

PT. ENDO INDONESIA

AR Address

Jl. Raya Menganti 14

Registration Date

Sep 29, 2020

Expiry Date

Jun 04, 2025

Product Type

Surgical Equipment

Electrosurgical cutting and coagulation device and accessories.

Non Radiation Electromedics

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