FDA UDI In Commercial Distribution 🇺🇸 United States

PlasmaKinetic

DI: 00821925039599 · Model: 744010 · Gyrus Acmi, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PlasmaKinetic
Primary DI
00821925039599
Version / Model
744010
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
6
Public Version Date
2023-11-06
Public Version Status
Update
Public Device Record Key
8dd2f43b-8ace-4723-a936-b46fd54b8e61

Device Description

PLASMAKINETIC SUPERPULSE SYSTEM Footswitch

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

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Primary 00821925039599

Premarket Submissions

Submission Number Supplement Number
K031085 000