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VISIANO 10-1 P S10 - Indonesia BPOM Medical Device Registration

VISIANO 10-1 P S10 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903020542. The device is manufactured by DERUNGS LICHT AG from Switzerland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GE OPERATIONS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : A
VISIANO 10-1 P S10
Analysis ID: AKL 10903020542

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

DERUNGS LICHT AG

Country of Origin

Switzerland

Authorized Representative

PT. GE OPERATIONS INDONESIA

AR Address

South Quarter Tower B, Lantai 18-19, JL. R.A. Kartini Kav. 8, Kelurahan Cilandak Barat, Kecamatan Cilandak, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, 12430

Registration Date

Mar 22, 2024

Expiry Date

Dec 19, 2028

Product Type

General Hospital Equipment and Other Individuals

AC-powered medical examination light.

Non Radiation Electromedics

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