FDA UDI In Commercial Distribution 🇺🇸 United States

KENEX

DI: 05055449415668 · Model: 1340/3/10 · KENEX (ELECTRO-MEDICAL) LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KENEX
Primary DI
05055449415668
Version / Model
1340/3/10
Catalog Number
1340/3/10
Company Name
KENEX (ELECTRO-MEDICAL) LIMITED
Labeler DUNS
217421064
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-07-11
Public Version
1
Public Version Date
2023-07-19
Public Version Status
New
Public Device Record Key
4f763a42-fa95-4e3a-8bdf-03c15b3e36e1

Device Description

1340/3/10 Mob Tableside Control Pedestal(10x25mm section)

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
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IWX Barrier, Control Panel, X-Ray, Movable

GMDN Terms

Code Name
38373 Radiation shielding panel, portable/mobile

Identifiers

Type ID
Primary 05055449415668