FDA UDI In Commercial Distribution 🇺🇸 United States

PlasmaBlade(TM)

DI: 20643169175109 · Model: PS300-001 · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
4

Basic Information

Brand Name
PlasmaBlade(TM)
Primary DI
20643169175109
Version / Model
PS300-001
Company Name
MEDTRONIC, INC.
Labeler DUNS
030200852
Distribution Status
In Commercial Distribution
Device Count in Pkg
4
Record Status
Published
Publish Date
2016-05-14
Public Version
4
Public Version Date
2019-03-12
Public Version Status
Update
Public Device Record Key
a3c23677-20f7-45e4-91eb-2aab94539d16

Device Description

PLASMABLADE PS300-001 TONSIL 4PK

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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GEI ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES

GMDN Terms

Code Name
61869 Open-surgery electrosurgical handpiece/electrode, monopolar, single-use

Identifiers

Type ID
Primary 20643169175109
Unit of Use 00643169175105

Customer Contacts