FDA UDI In Commercial Distribution 🇺🇸 United States

CON LEAD 18G

DI: 03665134000288 · Model: KRNG.AB.18 · KOELIS
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
5

Basic Information

Brand Name
CON LEAD 18G
Primary DI
03665134000288
Version / Model
KRNG.AB.18
Company Name
KOELIS
Labeler DUNS
290318455
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2023-04-05
Public Version
1
Public Version Date
2023-04-13
Public Version Status
New
Public Device Record Key
272fda13-d6f6-4701-9ad5-7fa9b623d8fa

Device Description

Needle guide compatible with the abdominal 2D ultrasound probe. It is made of two parts. One part is fixed on the ultrasound probe. The other removable part is perforated and inserted in the first part to guide the needle. The device is designed to guide needles with a diameter from 17G to 20G. The guides are reusable after appropriate procedure. They are not delivered in sterile condition

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
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
ITX Transducer, Ultrasonic, Diagnostic

GMDN Terms

Code Name
60734 Needle guide, reusable

Identifiers

Type ID
Unit of Use 03665134000189
Primary 03665134000288

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K171040 000