FDA UDI In Commercial Distribution 🇺🇸 United States

KENEX

DI: 05055449416009 · Model: 1501/D · KENEX (ELECTRO-MEDICAL) LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KENEX
Primary DI
05055449416009
Version / Model
1501/D
Catalog Number
1501/D
Company Name
KENEX (ELECTRO-MEDICAL) LIMITED
Labeler DUNS
217421064
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
1
Public Version Date
2022-12-16
Public Version Status
New
Public Device Record Key
2398d6f8-74d7-434b-a53a-cbf5ec3b75ab

Device Description

Hydraulic Patients Chair

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
FRK Chair, Examination And Treatment

GMDN Terms

Code Name
40697 Diagnostic x-ray system chair

Identifiers

Type ID
Primary 05055449416009