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xeo SA - EUDAMED Registration 00816722021113

Access comprehensive regulatory information for xeo SA in the European Union medical device market through Pure Global AI's free database. This Class IIb device is registered with EU EUDAMED under Primary DI 00816722021113 and manufactured by Cutera, Inc. in United States.

This page provides complete registration details including trade name (xeo SA), manufacturer information, authorized representative details, competent authority (DE/CA09 - Staatliches Gewerbeaufsichtsamt Hannover), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.

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EUDAMED Official Data
Class IIb
00816722021113
Yes
xeo SA
Trade Name: xeo SA
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Device Description (EMDN)

MULTI–PLATFORM LASER

Device Classification
Risk Class
Class IIb
CND Nomenclatures Code
Z12011019
Trade Name
xeo SA
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
00816722021113
Basic UDI
B-00816722021113
Active Status
Yes
Manufacturer
Manufacturer Name
Cutera, Inc.
Country
United States
Country Type
NON_EU
Address
3240 Bayshore Blvd Brisbane
Email
info@cutera.com
Authorized Representative
SRN
DE-AR-000005430
Country
Germany
Address
41 Schiffgraben Hannover
Email
info@mdssar.com
Regulatory Information
Competent Authority
DE/CA09 - Staatliches Gewerbeaufsichtsamt Hannover
Applicable Legislation
MDD (Directive 93/42/EEC on Medical Devices)
Placed On The Market
France
Market Available
Belgium:2004-05-01~None, France:2004-05-01~None, Germany:2004-05-01~None, Ireland:2004-05-01~None, Italy:2004-05-01~None, Latvia:2004-05-01~None, Netherlands:2004-05-01~None, Poland:2004-05-01~None, Romania:2004-05-01~None, Spain:2004-05-01~None, Sweden:2004-05-01~None, Türkiye:2004-05-01~None
Device Characteristics
Human Tissues
No
Animal Tissues
No