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XION EndoSTROBE PL Spectar - Indonesia BPOM Medical Device Registration

XION EndoSTROBE PL Spectar is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801123551. The device is manufactured by XION GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRIADI LINTAS PERSADA.

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BPOM Registered
Risk Class Kelas Resiko : B
XION EndoSTROBE PL Spectar
Analysis ID: AKL 20801123551

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

XION GMBH

Country of Origin

Germany

Authorized Representative

PT. TRIADI LINTAS PERSADA

AR Address

Ruko Exclusive Raden Inten Jl. Raden Inten II No. 80 Kav. 5

Registration Date

Jul 27, 2022

Expiry Date

Dec 31, 2024

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Radiation Electromedics

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