FDA UDI In Commercial Distribution 🇺🇸 United States

FINESSE

DI: H671FIN2200 · Model: Finesse+, 230VAC · UTAH MEDICAL PRODUCTS, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
FINESSE
Primary DI
H671FIN2200
Version / Model
Finesse+, 230VAC
Catalog Number
FIN-220
Company Name
UTAH MEDICAL PRODUCTS, INC.
Labeler DUNS
094651270
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
5f4cd26b-a584-4b10-8e7c-2dd227370830

Device Description

Electrosurgical Generator with Integrated Smoke Evacuation System, 230 VAC

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
Yes
Has Lot/Batch Number
No
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
HGI Electrocautery, Gynecologic (And Accessories)

GMDN Terms

Code Name
11490 Electrosurgical system generator

Identifiers

Type ID
Primary H671FIN2200

Customer Contacts

Phone
800-533-4984

Premarket Submissions

Submission Number Supplement Number
K123310 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 230 Volt AC

Storage Conditions

Type
Handling Environment Atmospheric Pressure
Temperature Range
50 – 106 KiloPascal
Type
Handling Environment Humidity
Temperature Range
10 – 93 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
-40 – 70 Degrees Celsius