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BLOW 165 DUO - Indonesia BPOM Medical Device Registration

BLOW 165 DUO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801913340. 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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BPOM Registered
Risk Class Kelas Resiko : B
BLOW 165 DUO

SOPRO 165 DUO

Analysis ID: AKL 20801913340

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

Jun 21, 2019

Expiry Date

Mar 25, 2024

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories

Non Radiation Electromedics

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