Model: 221800-000240
Catalog: 221800-000240
DI: 14026704942494
Status: New
MRI: Labeling does not contain MRI Safety Information
Single-use: Yes
Rx: No
OTC: No
First Published: 2026-05-15
Current Version: 2026-05-25
Sterilization
Device Sterile:
Yes
Sterilization Prior To Use:
No
Regulatory & Distribution
Record Status:
Published
Version Number:
1
Record Key:
9f41a809-e7d0-489c-95f4-74e34efc276e
Distribution Status:
In Commercial Distribution
DUNS Number:
002348191
Device Count:
1
DM Exempt:
No
Premarket Exempt:
No
HCT/P:
No
Kit:
No
Combination Product:
No
Lot/Batch Tracked:
Yes
Serial Number Tracked:
No
Manufacturing Date Tracked:
No
Expiration Date Tracked:
Yes
Donation ID Number Tracked:
No
Labeled Contains NRL:
No
Labeled No NRL:
No
Identifiers
Item #1 - Pkg Type:
CT
Item #1 - Device ID:
24026704942491
Item #1 - Pkg Status:
In Commercial Distribution
Item #1 - Pkg Quantity:
12
Item #1 - Device ID Type:
Package
Item #1 - Contains DINumber:
04026704942497
Item #1 - Device ID Issuing Agency:
GS1
Item #2 - Pkg Type:
BX
Item #2 - Device ID:
04026704942497
Item #2 - Pkg Status:
In Commercial Distribution
Item #2 - Pkg Quantity:
50
Item #2 - Device ID Type:
Package
Item #2 - Contains DINumber:
14026704942494
Item #2 - Device ID Issuing Agency:
GS1
Item #3 - Device ID:
14026704942494
Item #3 - Device ID Type:
Primary
Item #3 - Device ID Issuing Agency:
GS1
GMDN
Code: 45603
Name: Single-administration urethral drainage catheter
Definition:
A sterile, flexible tube intended to be inserted one-time through the urethra to the urinary bladder, by the patient/user or a healthcare provider, to provide urine drainage, typically for an individual who is physiologically incapable of voiding. It is typically made of polyvinyl chloride (PVC), and may be coated with a lubricating substance (e.g., acquires a smooth and mucous surface when brought in contact with water). The distal end can have various tip designs [e.g., open-ended, rounded with a side hole(s)], and the proximal end typically connects to a urine collection container. This is a single-use device.
FDA Product Codes
EZC
CATHETER, COUDE
Premarket Submissions
Submission Number:
K222279
Supplement Number:
000