FDA UDI In Commercial Distribution 🇺🇸 United States

CellFX

DI: 00850003231600 · Model: FG5004-01 · Pulse Biosciences, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CellFX
Primary DI
00850003231600
Version / Model
FG5004-01
Catalog Number
CTT0152
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
63475d22-7835-4f8c-b88c-ca20fdcf3a50

Device Description

CellFX Treatment Tip – 1.5 x 1.5mm [2mm]

Device Characteristics

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
Yes
Sterilization Methods
Ethylene Oxide

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Package 10850003231607
Primary 00850003231600

Premarket Submissions

Submission Number Supplement Number
K203299 000