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VISIOMULTI Superelastic and Glideable Guide Wire Made of Nitinol, Stiff - Indonesia BPOM Medical Device Registration

VISIOMULTI Superelastic and Glideable Guide Wire Made of Nitinol, Stiff is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804810116. The device is manufactured by UROVISION GESELLSCHAFT FรœR MEDIZINISCHE TECHNOLOGIE-TRANSFER MBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SINAR MULIA INDOMEDIKA.

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Risk Class Kelas Resiko : B
VISIOMULTI Superelastic and Glideable Guide Wire Made of Nitinol, Stiff
Analysis ID: AKL 20804810116

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. SINAR MULIA INDOMEDIKA

AR Address

Ruko Premier Park 2 Block : AB No.26, Modernland Cikokol Tangerang

Registration Date

Dec 26, 2022

Expiry Date

Jan 31, 2027

Product Type

Gastroenterology-Surgical Urology Equipment

Manual gastroenterology-urology surgical instrument and accessories

Non Electromedic Sterile

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