FDA UDI In Commercial Distribution 🇺🇸 United States

PlasmaKinetic

DI: 00821925039520 · Model: 786500 · Gyrus Acmi, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PlasmaKinetic
Primary DI
00821925039520
Version / Model
786500
Company Name
Gyrus Acmi, Inc.
Labeler DUNS
007198742
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-04
Public Version
5
Public Version Date
2023-11-03
Public Version Status
Update
Public Device Record Key
a9ac69fa-0ce9-468a-b347-032a28bba0bb

Device Description

PLASMAKINETIC SUPERPLUSE SYSTEM PK Button Front Loading Electrode

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
No

Product Codes

Code Name
FAS ELECTRODE, ELECTROSURGICAL, ACTIVE, UROLOGICAL

GMDN Terms

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

Identifiers

Type ID
Package 00821925011519
Primary 00821925039520

Premarket Submissions

Submission Number Supplement Number
K093181 000