FDA UDI In Commercial Distribution 🇺🇸 United States

CellFX

DI: 00850003231389 · Model: FG2100-01 · Pulse Biosciences, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CellFX
Primary DI
00850003231389
Version / Model
FG2100-01
Catalog Number
CFX10
Company Name
Pulse Biosciences, Inc.
Labeler DUNS
080114073
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-02-26
Public Version
2
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
ac436965-81a9-421e-b5b4-3a45715a05e8

Device Description

CellFX Console

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
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
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Primary 00850003231389

Premarket Submissions

Submission Number Supplement Number
K203299 000