FDA UDI In Commercial Distribution 🇺🇸 United States

BiSurge

DI: 00877972006619 · Model: 620-163-920 · GENICON, INC.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BiSurge
Primary DI
00877972006619
Version / Model
620-163-920
Company Name
GENICON, INC.
Labeler DUNS
079805400
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-10-11
Public Version
5
Public Version Date
2020-01-09
Public Version Status
Update
Public Device Record Key
ba8d472a-5b16-4a22-a710-4eb8726feddb

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
GEA Cannula, Surgical, General & Plastic Surgery
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
42412 Laparoscopic access cannula, single-use
57944 Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

Identifiers

Type ID
Primary 00877972006619

Premarket Submissions

Submission Number Supplement Number
K041968 000