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OCUGAS C3F8 - ARCSA Registration 2c54db012ef013619a25d540e1c9bca3

Access comprehensive regulatory information for OCUGAS C3F8 in the Ecuador medical device market through Pure Global AI's free database. This III medical device is registered under ARCSA ID 2c54db012ef013619a25d540e1c9bca3 and manufactured by D.O.R.C. DUTCH OPHTALMIC RESEARCH CENTER (INTERNATIONAL) B.V. (DORC). The device was registered on December 07, 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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ARCSA Official Data
III
2c54db012ef013619a25d540e1c9bca3
OCUGAS C3F8
ARCSA ID: 2c54db012ef013619a25d540e1c9bca3
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Device Classification
Risk Class
III
Product Type
Invasive
Brand Name
OCUGAS DORC
Commercial Name
OPHTHALMIC GASES, VITREOUS CAVITY, SULPHUR HEXAFLUORIDE
Registration Information
Analysis ID
2c54db012ef013619a25d540e1c9bca3
Registration Date
December 07, 2022
Expiration Date
December 07, 2027
Product Use

INTERMEDIATE TAMPONADE AFTER OPERATIVE TREATMENT OF SEVERE RETINAL DETACHMENT.

Manufacturer
City
SOUTHLAND
Country
NETHERLANDS
Address
SCHEIJDELVEWEG 2, 3214 VN ZUIDLAND
Product Owner
Name
D.O.R.C. DUTCH OPHTALMIC RESEARCH CENTER (INTERNATIONAL) B.V. (DORC)
Country
NETHERLANDS
Authorized Representative
Address
AV. DE LOS SHYRIS N32-21 AND AV. ELOY ALFARO. CENTRAL PARK BUILDING. 5TH FLOOR. OF. 509
Phone
23801252