FDA UDI In Commercial Distribution 🇺🇸 United States

Force Triverse

DI: 10884524000084 · Model: FT3000 · Covidien LP
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Force Triverse
Primary DI
10884524000084
Version / Model
FT3000
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
11
Public Version Date
2025-06-24
Public Version Status
Update
Public Device Record Key
79e50db4-1b78-4c3e-9ac2-df62302741b6

Device Description

Electrosurgical Device Holster;For use with maximum peak voltage of 4000 V

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
Yes
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
57944 Endoscopic electrosurgical handpiece/electrode, bipolar, single-use

Identifiers

Type ID
Package 20884524000081
Primary 10884524000084

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K051627 000
K150735 000

Device Sizes

Type Value Unit Text
Length 10 Feet