FDA UDI In Commercial Distribution 🇺🇸 United States

FINESSE

DI: H671FIN8000 · Model: Starter Kit · 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
H671FIN8000
Version / Model
Starter Kit
Catalog Number
FIN-800
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
5
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
94b61bdd-af53-4b3d-a8ff-b64d2eb42ac0

Device Description

Starter Kit, Including 1 ea. DLS-200, 5 ea. ESU-305, 1 ea. ESU-501, 15 ea. ESU-502, & 10 ea. ES-1179

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
No
Has Expiration Date
Yes
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 H671FIN8000

Customer Contacts

Phone
800-533-4984

Premarket Submissions

Submission Number Supplement Number
K123310 000