FDA UDI In Commercial Distribution 🇺🇸 United States

PANA SPRAY Plus

DI: 04589551393367 · Model: PANA SPRAY Plus · NAKANISHI INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
PANA SPRAY Plus
Primary DI
04589551393367
Version / Model
PANA SPRAY Plus
Company Name
NAKANISHI INC.
Labeler DUNS
690710546
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-24
Public Version
1
Public Version Date
2025-10-02
Public Version Status
New
Public Device Record Key
864f898e-fd38-463e-a00c-a5f43d3bdb49

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
No
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EFB Handpiece, air-powered, dental

GMDN Terms

Code Name
15772 Surgical instrument maintenance lubricant

Identifiers

Type ID
Primary 04589551393367

Premarket Submissions

Submission Number Supplement Number
K163483 000