Cranial Perforator - FDA Registration 2565281dba47dabcfdd526baf4e6c72b
Access comprehensive regulatory information for Cranial Perforator in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2565281dba47dabcfdd526baf4e6c72b and manufactured by Acra-Cut Inc., USA. The device was registered on June 26, 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
2565281dba47dabcfdd526baf4e6c72b
Cranial Perforator
FDA ID: 2565281dba47dabcfdd526baf4e6c72b
Device Classification
Brand Name
ACRA-CUT
Registration Information
Analysis ID
2565281dba47dabcfdd526baf4e6c72b
Registration Date
June 26, 2022
Manufacturer
Authorized Representative

