FDA UDI In Commercial Distribution 🇺🇸 United States

Jenx

DI: 05056235209515 · Model: SB31 001 · JENX LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Jenx
Primary DI
05056235209515
Version / Model
SB31 001
Company Name
JENX LIMITED
Labeler DUNS
291659639
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-09-29
Public Version
2
Public Version Date
2023-10-18
Public Version Status
Update
Public Device Record Key
7387a416-2183-4b8c-8234-651a7f2fb5e3

Device Description

Arched Foam Pad

Device Characteristics

Single Use
No
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
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
INW Table, Mechanical

GMDN Terms

Code Name
13356 Wheelchair/chair/stander occupant restraint/support

Identifiers

Type ID
Primary 05056235209515