FDA UDI In Commercial Distribution 🇺🇸 United States

PlasmaKinetic

DI: 00821925010802 · Model: 3900 · Gyrus ACMI, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
PlasmaKinetic
Primary DI
00821925010802
Version / Model
3900
Company Name
Gyrus ACMI, LLC
Labeler DUNS
007198742
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-12
Public Version
8
Public Version Date
2024-09-02
Public Version Status
Update
Public Device Record Key
d9e4f63a-c69e-415d-8e30-13868460a471

Device Description

PK 3 Pin Connector Cord "3900 PK REUSABLE CONNECTOR CABLE (3-pin)"

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
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Primary 00821925010802

Premarket Submissions

Submission Number Supplement Number
K031085 000