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DUO FULL HD S195 - Indonesia BPOM Medical Device Registration

DUO FULL HD S195 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801021677. The device is manufactured by PUFF from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is VERSACON MEDICAL.

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Risk Class Kelas Resiko : B
DUO FULL HD S195
Analysis ID: AKL 20801021677

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

PUFF

Country of Origin

France

Authorized Representative

VERSACON MEDICAL

AR Address

JL ANGGREK NELI MURNI BLOK C NO 30-30 A, PALMERAH

Registration Date

Mar 31, 2020

Expiry Date

Mar 25, 2024

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories

Non Radiation Electromedics

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