M3/M4/CRANIOFACIAL MODULAR FIXATION SYSTEM™ CFX™ / CRANIOMAXILOFACIAL TRAUMA FIXATION SYSTEM™. - DIGEMID Registration DM16005E
Access comprehensive regulatory information for M3/M4/CRANIOFACIAL MODULAR FIXATION SYSTEM™ CFX™ / CRANIOMAXILOFACIAL TRAUMA FIXATION SYSTEM™. in the Peru medical device market through Pure Global AI's free database. This medical device is registered under DIGEMID ID DM16005E and manufactured by OSTEOMED. The device was registered on December 28, 2018.
This page provides complete registration details including product type (MEDICAL DEVICE), manufacturer information, authorized representative details, and regulatory compliance data from the official Peru DIGEMID medical device database. Pure Global AI offers free access to Peru's complete medical device registry.
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DIGEMID Official Data
DM16005E
M3/M4/CRANIOFACIAL MODULAR FIXATION SYSTEM™ CFX™ / CRANIOMAXILOFACIAL TRAUMA FIXATION SYSTEM™.
DIGEMID ID: DM16005E
Device Classification
Product Type
MEDICAL DEVICE
Registration Information
Analysis ID
DM16005E
Registration Date
December 28, 2018
Expiration Date
December 28, 2023
Creation Date
February 23, 2023
Manufacturer
Name
OSTEOMEDAuthorized Representative

