FDA UDI In Commercial Distribution 🇺🇸 United States

BiSurge

DI: 00877972006275 · Model: 633-005-920 · GENICON, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BiSurge
Primary DI
00877972006275
Version / Model
633-005-920
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
2019-04-23
Public Version Status
Update
Public Device Record Key
8955bfe4-2773-4289-916a-869876331f59

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
57944 Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

Identifiers

Type ID
Primary 00877972006275

Premarket Submissions

Submission Number Supplement Number
K041968 000