FDA product code GEI

Electrosurgical, Cutting & Coagulation & Accessories

General, Plastic Surgery·Class 2·21 CFR 878.4400
US regulatory classifications
US Product Code (FDA)
GEI
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US Risk Class (FDA)
Class 2
US Regulation (CFR)
21 CFR 878.4400
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Medical specialty
General, Plastic Surgery
Device characteristics
GMP exempt
No
Implantable
No
Life-sustaining
No
Third party review
Eligible
Definition

Validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission if the device is reusable and has specific design features (please refer to Table 2 of 82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

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About this record

Electrosurgical, Cutting & Coagulation & Accessories is a medical device type in the General, Plastic Surgery specialty. This page includes real-world medical device registration data worldwide for this device type, with registrations from US FDA, Brazil ANVISA, and other global markets.

View regulatory classifications, recent 510(k) clearances, active device registrations, and similar products registered globally under this device category. Pure Global AI's free directory provides comprehensive worldwide registration intelligence across 7,000+ medical device types and 21 specialties.