FDA UDI In Commercial Distribution 🇺🇸 United States

Pana-Max2 M4

DI: 04589551385720 · Model: Pana-Max2 M4 · NAKANISHI INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Pana-Max2 M4
Primary DI
04589551385720
Version / Model
Pana-Max2 M4
Company Name
NAKANISHI INC.
Labeler DUNS
690710546
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-09
Public Version
1
Public Version Date
2023-03-17
Public Version Status
New
Public Device Record Key
cae6bc6f-c172-4b1b-8076-c999d31ef55d

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
EFB Handpiece, air-powered, dental

GMDN Terms

Code Name
66244 Dental surgical power tool motorized handpiece/set, pneumatic

Identifiers

Type ID
Direct Marking 04560264537712
Primary 04589551385720

Premarket Submissions

Submission Number Supplement Number
K203791 000