FDA UDI In Commercial Distribution 🇺🇸 United States

Surgic Pro2 NON-OPT

DI: 04589551392889 · Model: Surgic Pro2 NON-OPT · NAKANISHI INC.
Product Codes
1
GMDN Terms
3
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Surgic Pro2 NON-OPT
Primary DI
04589551392889
Version / Model
Surgic Pro2 NON-OPT
Company Name
NAKANISHI INC.
Labeler DUNS
690710546
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-08-26
Public Version
1
Public Version Date
2025-09-03
Public Version Status
New
Public Device Record Key
4074b2a3-5086-4d40-b77b-b8b383cc07e2

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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
EBW Controller, foot, handpiece and cord

GMDN Terms

Code Name
36336 Foot-switch, electrical
41264 Surgical power tool system control unit, line-powered
66227 Dental surgical power tool motor, electric

Identifiers

Type ID
Primary 04589551392889