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BLOW COMEG SYMBIOZ LED - Indonesia BPOM Medical Device Registration

BLOW COMEG SYMBIOZ LED is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801615785. The device is manufactured by BLOW COMEG. from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. VERSACON MEDICAL.

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Risk Class Kelas Resiko : B
BLOW COMEG SYMBIOZ LED

SOPRO COMEG SYMBIOZ LED

Analysis ID: AKL 20801615785

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

BLOW COMEG.

Country of Origin

France

Authorized Representative

PT. VERSACON MEDICAL

AR Address

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

Registration Date

Apr 17, 2020

Expiry Date

Mar 25, 2024

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Radiation Electromedics

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