FDA UDI In Commercial Distribution 🇺🇸 United States

PlasmaBladeTM

DI: 00643169507869 · Model: PS210-030S · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PlasmaBladeTM
Primary DI
00643169507869
Version / Model
PS210-030S
Company Name
MEDTRONIC, INC.
Labeler DUNS
030200852
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-16
Public Version
4
Public Version Date
2021-11-22
Public Version Status
Update
Public Device Record Key
46ee5f17-b2d3-4f98-ae9f-367f7a2258bc

Device Description

PLASMABLADE PS210-030S 3.0S LOCK

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 00643169507869

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K093695 000