FDA UDI In Commercial Distribution 🇺🇸 United States

Jenx (Daytot)

DI: 05056235223290 · Model: 207-612 · JENX LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Jenx (Daytot)
Primary DI
05056235223290
Version / Model
207-612
Company Name
JENX LIMITED
Labeler DUNS
291659639
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-08-08
Public Version
1
Public Version Date
2025-08-18
Public Version Status
New
Public Device Record Key
a40ff2e8-8a76-4da2-b878-25279d288dee

Device Description

Joey Size 2 Fabric Cover (spare)

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
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
CCX Support, Patient Position

GMDN Terms

Code Name
31166 Assistive crawler/mobility board

Identifiers

Type ID
Primary 05056235223290