FDA UDI In Commercial Distribution 🇺🇸 United States

NeckCare Device

DI: 05694230564033 · Model: NS-110X2 · NeckCare Holding ehf
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NeckCare Device
Primary DI
05694230564033
Version / Model
NS-110X2
Company Name
NeckCare Holding ehf
Labeler DUNS
500824286
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-30
Public Version
1
Public Version Date
2025-06-09
Public Version Status
New
Public Device Record Key
16a91db7-8a0a-4da8-a76b-e1d5e687a7e1

Device Description

The NeckCare Device is used to measure and record head motion during instructed head-neck movements.

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
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KQX Goniometer, Ac-Powered

GMDN Terms

Code Name
33652 Electronic goniometer/kinesiology sensor

Identifiers

Type ID
Primary 05694230564033
Previous 05694230564019

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
-25 – 70 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
0 – 90 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-25 – 70 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
0 – 90 Percent (%) Relative Humidity