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RUTISIDE - Lighting device for surgical instruments - Indonesia BPOM Medical Device Registration

RUTISIDE - Lighting device for surgical instruments is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603324980. The device is manufactured by SWAN MEDICAL S.L. from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. AMPM HEALTHCARE INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
RUTISIDE - Lighting device for surgical instruments
Analysis ID: AKL 21603324980

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SWAN MEDICAL S.L.

Country of Origin

Spain

Authorized Representative

PT. AMPM HEALTHCARE INDONESIA

AR Address

Jl.Cengkeh Kav.16 No.29-30

Registration Date

Sep 12, 2023

Expiry Date

Feb 01, 2028

Product Type

Surgical Equipment

Surgical lamp.

Non Electromedic Sterile

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