FDA UDI In Commercial Distribution 🇺🇸 United States

NanoSurge

DI: 00877972006190 · Model: 520-063-910 · GENICON, INC.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NanoSurge
Primary DI
00877972006190
Version / Model
520-063-910
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
5
Public Version Date
2020-01-09
Public Version Status
Update
Public Device Record Key
afb94875-3feb-403e-a4b5-2b1423c9f23c

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
GEA Cannula, Surgical, General & Plastic Surgery

GMDN Terms

Code Name
42412 Laparoscopic access cannula, single-use
58039 Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

Identifiers

Type ID
Primary 00877972006190

Premarket Submissions

Submission Number Supplement Number
K061417 000