FDA UDI In Commercial Distribution 🇺🇸 United States

X-Surge

DI: 00877972006725 · Model: 590-005-014 · GENICON, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
X-Surge
Primary DI
00877972006725
Version / Model
590-005-014
Company Name
GENICON, INC.
Labeler DUNS
079805400
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-03
Public Version
2
Public Version Date
2019-02-21
Public Version Status
Update
Public Device Record Key
282a684d-5208-42ea-9fc0-748f4dc75dd7

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
58039 Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

Identifiers

Type ID
Primary 00877972006725

Premarket Submissions

Submission Number Supplement Number
K171752 000