VISE CYSTO-NEPHRO VIDEOSCOPE OLYMPUS CYF TYPE V2 - FDA Registration 15db44ce26014c36db2818f95c64897c
Access comprehensive regulatory information for VISE CYSTO-NEPHRO VIDEOSCOPE OLYMPUS CYF TYPE V2 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 15db44ce26014c36db2818f95c64897c and manufactured by Shirakawa Olympus Co.,Ltd. The device was registered on September 16, 2022.
This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.
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FDA Official Data
15db44ce26014c36db2818f95c64897c
VISE CYSTO-NEPHRO VIDEOSCOPE OLYMPUS CYF TYPE V2
FDA ID: 15db44ce26014c36db2818f95c64897c
Local name: VISERA CYSTO-NEPHRO VIDEOSCOPE OLYMPUS CYF TYPE V2
Device Classification
Brand Name
Olympus
Registration Information
Analysis ID
15db44ce26014c36db2818f95c64897c
Registration Date
September 16, 2022
Manufacturer
Authorized Representative

