FDA UDI In Commercial Distribution 🇺🇸 United States

GeniSurge

DI: 00877972001980 · Model: 533-005-905 · GENICON, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GeniSurge
Primary DI
00877972001980
Version / Model
533-005-905
Company Name
GENICON, INC.
Labeler DUNS
079805400
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-05
Public Version
4
Public Version Date
2019-02-21
Public Version Status
Update
Public Device Record Key
9ced13c2-6bbd-4c6e-99b9-3e425bcff526

Device Characteristics

Single Use
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

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 00877972001980

Premarket Submissions

Submission Number Supplement Number
K061417 000