DIAMOND™ Co-Cr-Mo Bipolar Head - FDA Registration 0d869c3e25b678803c7d14ae93d01a2d
Access comprehensive regulatory information for DIAMOND™ Co-Cr-Mo Bipolar Head in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0d869c3e25b678803c7d14ae93d01a2d and manufactured by Tianjin Zhengtian Medical Instrument Co., Ltd.. The device was registered on June 30, 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
0d869c3e25b678803c7d14ae93d01a2d
DIAMOND™ Co-Cr-Mo Bipolar Head
FDA ID: 0d869c3e25b678803c7d14ae93d01a2d
Device Classification
Brand Name
IRENE Brand
Registration Information
Analysis ID
0d869c3e25b678803c7d14ae93d01a2d
Registration Date
June 30, 2022
Manufacturer
Authorized Representative

