DEVICE: Urocare® Tubing White-Rubber with Connector 0.31" ID x 18" (00792293060167)
Device Identifier (DI) Information
Urocare® Tubing White-Rubber with Connector 0.31" ID x 18"
6016
In Commercial Distribution
6016
UROCARE PRODUCTS, INC.
6016
In Commercial Distribution
6016
UROCARE PRODUCTS, INC.
TUBING, URINE COLLECTION, OSTOMY, WHITE-RUBBER, CONNECTOR, REUSABLE
Features “Reverse-Grip” technology and graduated barbs to provide a secure hold on most standard sized drainage or extension tubing. May be used to connect Uro-Con® or Uro-Cath® male external catheters, Foley® indwelling catheters and reusable or disposable urinary drainage bags, bottles or other urinary and ostomy appliances. Provides a snug fit on most standard sized drainage ports/outlets while resisting kinks.
DEHP-Free and Latex-Free.
Includes #6010 Large Tubing Connector preassembled.
Device Characteristics
Labeling does not contain MRI Safety Information | |
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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? |
---|---|---|---|---|
58921 | Non-wearable adult urine collection bag, open-ended |
A flexible plastic pouch designed to connect to a urinary catheter or a urinary condom catheter to collect discharged urine from an adult/adolescent patient; it is designed with an opening for urine drainage. The device is not directly attached to the patient. This is a single-use device.
|
Active | false |
40504 | Hand-held urinal, reusable |
A portable, hand-held container intended to be directly urinated into by a patient for excretory purposes; it may be specific to male or female patients, or unisex. It is typically in the form of a bottle with a handle, or a bag, or pouch; it may include a noninvasive funnel and tubing, and may have a drain with a stopper in it to facilitate emptying. It is not intended to be worn by the patient. This is a reusable device.
|
Active | false |
34929 | Urinary incontinence penis sheath/port, single-use |
A device intended to be worn on or over the penis by an incontinent patient to channel urine from the penis, via a tube, into a collection bag. It consists of a penis-worn sheath (e.g., condom-catheter) or adhesive port (e.g., glans penis attachment), and may include a portion of tubing; the bag is not included. This device provides an alternative to inserting a catheter through the urethra, especially when difficulty is encountered in insertion or retention. It may be used to treat urinary incontinence or for non-ambulatory patients. This is a single-use device.
|
Active | false |
58924 | Open-ended wearable urine collection bag, non-sterile |
A non-sterile flexible plastic pouch designed to connect to a urinary catheter, a urinary condom catheter, or a urostomy bag, and to be strapped to the leg of a patient to collect discharged urine; it is designed with an opening for urine drainage. Also known as a leg bag, it is worn on the body to facilitate patient mobility. This is a single-use device.
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Obsolete | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
NNX | Device, Incontinence, Urosheath Type, Non-Sterile |
FAQ | Bag, Urine Collection, Leg, For External Use, Sterile |
NNW | Bag, Urine Collection, Leg, For External Use, Non-Sterile |
KNX | Collector, Urine, (And Accessories) For Indwelling Catheter |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
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Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
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No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
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Lumen/Inner Diameter: 0.31 Inch |
Length: 18 Inch |
Outer Diameter: 0.38 Inch |
Weight: 0.08 Pound |
Device Record Status
ab32f485-a487-46a6-84b4-3f328704a34b
June 10, 2022
7
May 31, 2018
June 10, 2022
7
May 31, 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 |
---|---|---|---|---|---|
10792293060164 | 12 | 00792293060167 | In Commercial Distribution | Case |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
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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