FDA UDI In Commercial Distribution 🇺🇸 United States

KING

DI: 00663427001113 · Model: KM-1320/E · Kego Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KING
Primary DI
00663427001113
Version / Model
KM-1320/E
Catalog Number
KM-1320
Company Name
Kego Corporation
Labeler DUNS
208120423
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-07
Public Version
1
Public Version Date
2023-11-15
Public Version Status
New
Public Device Record Key
f80d0128-adfb-4077-9016-a3bcda21514b

Device Description

KING Jumper w/TP Connector, Qty 3, 20 cm (8"), 3 Colour, R/BL/G

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
IKD Cable, Electrode

GMDN Terms

Code Name
35562 Electrocardiographic lead set, reusable

Identifiers

Type ID
Primary 00663427001113