FDA UDI In Commercial Distribution 🇺🇸 United States

Neuropen

DI: 00384700100018 · Model: NT0100 · OWEN MUMFORD LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Neuropen
Primary DI
00384700100018
Version / Model
NT0100
Company Name
OWEN MUMFORD LIMITED
Labeler DUNS
217266915
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-03
Public Version
1
Public Version Date
2019-10-11
Public Version Status
New
Public Device Record Key
740713d5-5237-42a2-be4e-7f02a5fe820c

Device Description

Non sterile, sensory neuropathy screening device

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GXB Esthesiometer

GMDN Terms

Code Name
61581 Pressure algometer/aesthesiometer, mechanical

Identifiers

Type ID
Package 00384700100032
Primary 00384700100018

Customer Contacts

Phone
770-977-2226

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 40 Degrees Celsius