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IMMISEAL DURAL SEALANT SYSTEM - ARCSA Registration d34b9401e58c7e4419364e0eff172390

Access comprehensive regulatory information for IMMISEAL DURAL SEALANT SYSTEM in the Ecuador medical device market through Pure Global AI's free database. This IV medical device is registered under ARCSA ID d34b9401e58c7e4419364e0eff172390 and manufactured by MEDPRIN BIOTECH GMBH. The device was registered on August 30, 2022.

This page provides complete registration details including product type (Invasive), manufacturer information, authorized representative details, and regulatory compliance data from the official Ecuador ARCSA medical device database. Pure Global AI offers free access to Ecuador's complete medical device registry.

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IV
d34b9401e58c7e4419364e0eff172390
IMMISEAL DURAL SEALANT SYSTEM
ARCSA ID: d34b9401e58c7e4419364e0eff172390
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Device Classification
Risk Class
IV
Product Type
Invasive
Brand Name
IMMISEAL
Commercial Name
ADHESIVES
Sterilization Method
GAMMA RADIATION
Registration Information
Analysis ID
d34b9401e58c7e4419364e0eff172390
Registration Date
August 30, 2022
Expiration Date
August 30, 2027
Creation Date
August 30, 2022
Product Use

IMISESAL'S HARD SEALANT SYSTEM IT IS INDICATED TO PROVIDE A HERMETIC CLOSURE AFTER REPAIRING DURA MATER DEFECTS RESULTING FROM TRAUMATIC BRAIN TRAUMA, BRAIN TUMOR, CEREBROVASCULAR DISEASE, CONGENITAL DISEASE OF THE NERVOUS SYSTEM, POSTERIOR PHASA SURGERY, SPINAL CANAL DISEASE AND OTHER DURA MATER DEFECTS CAUSED IN VARIOUS NEUROSURGICAL PROCEDURES AND ACCIDENTS.

Manufacturer
City
FRANKFURT
Country
GERMANY
Address
GUTLEUTSTRAฮ’E 163-167, 60327 FRANKFURT AM MAIN, GERMANY
Product Owner
Name
MEDPRIN BIOTECH GMBH
Country
GERMANY
Authorized Representative
Address
MIGUEL GAVIRIA E9-36 AND 6 DECEMBER
Phone
987441384