FDA UDI In Commercial Distribution 🇺🇸 United States

Unimax

DI: 14714127866809 · Model: FPS133059 · UNIMAX MEDICAL SYSTEMS INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Unimax
Primary DI
14714127866809
Version / Model
FPS133059
Company Name
UNIMAX MEDICAL SYSTEMS INC.
Labeler DUNS
658122465
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2021-08-10
Public Version
1
Public Version Date
2021-08-18
Public Version Status
New
Public Device Record Key
6f004213-b46e-48a8-b03c-d72e12c44f24

Device Description

Monopolar spatula probe

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
Yes
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
58039 Endoscopic electrosurgical handpiece/electrode, monopolar, single-use

Identifiers

Type ID
Package 24714127866806
Primary 14714127866809
Unit of Use 04714127866802

Device Sizes

Type Value Unit Text
Outer Diameter 5 Millimeter
Length 33 Centimeter