DEVICE: Argyle (10884527006410)
Device Identifier (DI) Information
Argyle
8888256529
In Commercial Distribution
8888256529
Cardinal Health, Inc.
8888256529
In Commercial Distribution
8888256529
Cardinal Health, Inc.
Replogle Suction Catheter
Device Characteristics
| Labeling does not contain MRI Safety Information | |
| No | |
| No | |
| Yes | |
| No | |
| Yes | |
| No | |
| No | |
| No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
| GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
|---|---|---|---|---|
| 15270 | Sump drain |
A sterile, tube-like device that has a double lumen which is designed to establish a channel for the removal of fluids from a cavity by allowing air to enter the cavity through the smaller lumen which displaces fluid into the larger lumen. This is a single-use device.
|
Active | false |
FDA Product Code
[?]| Product Code | Product Code Name |
|---|---|
| BSY | CATHETERS, SUCTION, TRACHEOBRONCHIAL |
FDA Premarket Submission
| FDA Premarket Submission Number [?] | Supplement Number [?] |
|---|---|
| Premarket Submission Number Not Available/Not Released | |
Sterilization
Storage and Handling
[?]| Storage and Handling |
|---|
| Special Storage Condition, Specify: Keep Dry;AVOID DIRECT SUNLIGHT |
Clinically Relevant Size
[?]| Size Type Text |
|---|
| Length: 24 Inch |
| Catheter Gauge: 8 French |
Device Record Status
2699dff3-2771-45b1-9739-82266908257a
July 31, 2024
3
June 30, 2018
July 31, 2024
3
June 30, 2018
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]| Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
|---|---|---|---|---|---|
| 20884527006417 | 10 | 10884527006410 | 2025-12-31 | In Commercial Distribution | CASE |
Secondary DI
[?]| Issuing Agency [?] | Secondary DI Number |
|---|---|
| No Secondary DIs found | |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
No Customer Contact currently defined