FDA UDI In Commercial Distribution 🇺🇸 United States

DPNCheck

DI: 00816022023688 · Model: NC-DP2 · IMPULSE MEDICAL TECHNOLOGIES, 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
DPNCheck
Primary DI
00816022023688
Version / Model
NC-DP2
Company Name
IMPULSE MEDICAL TECHNOLOGIES, INC.
Labeler DUNS
080015502
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-01-09
Public Version
1
Public Version Date
2026-01-19
Public Version Status
New
Public Device Record Key
bb39629d-d2a2-45b2-92da-2df39380eb0d

Device Description

DPNCheck 2.0 Biosensor

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
No
Sterilization Prior Use
No

Product Codes

Code Name
JXE Device, Nerve Conduction Velocity Measurement

GMDN Terms

Code Name
11425 Electrode conductive medium

Identifiers

Type ID
Primary 00816022023688

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K041320 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-30 – 60 Degrees Celsius