FDA UDI In Commercial Distribution 🇺🇸 United States

Ligasure

DI: 10884524001678 · Model: LF0500 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ligasure
Primary DI
10884524001678
Version / Model
LF0500
Company Name
Covidien LP
Labeler DUNS
058614483
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
4
Public Version Date
2022-04-05
Public Version Status
Update
Public Device Record Key
c9faabe3-8ffc-4acb-a1d4-3dfb9b4dd760

Device Description

Tissue Fusion Footswitch, Orange

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
36336 Foot-switch, electrical

Identifiers

Type ID
Primary 10884524001678

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K051644 000

Storage Conditions

Type
Handling Environment Humidity
Temperature Range
0 – 75 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
-29 – 149 Degrees Fahrenheit