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Uro-Cath® Molded-Latex Male External Catheter, Extra-Large 40mm with Urofoam®-2
FDA UDIClass I (US FDA UDI)
Identity
- Trade Name
- Uro-Cath® Molded-Latex Male External Catheter, Extra-Large 40mm with Urofoam®-2 FDA UDI
- Generic Name
- Urinary incontinence penis sheath/port, single-use FDA UDI
- Device Name
- These male external catheters are commonly referred to as a “Molded-Latex” style because they are dipped from a single piece of latex without seams rather than assembled from multiple components. Each Uro-Cath® catheter has a thin, latex sheath section similar to a condom at one end—the part that is rolled over the head and shaft of the penis—and a heavier funnel-shaped, cup section at the other—where urine is drained from into a bag or other collection device—making them virtually “twist-proof” by their unique design. Uro-Cath® catheters range in size from 25mm, our smallest, to 40mm, our largest in 5mm increments to suit a variety of individual requirements. They are packaged individually in a window pouch allowing for quick, easy product identification without opening the pouch. The back side of the pouch contains detailed, illustrated, application instructions relative to the product purchased Contains: 1 Uro-Cath® Male External Catheter, 1 Urofoam®-2 Double-Sided Adhesive Foam Strip, Illustrated, application instructions on back of pouch/package FDA UDI
- Model / Reference
- 522140 FDA UDI
- Description
- These male external catheters are commonly referred to as a “Molded-Latex” style because they are dipped from a single piece of latex without seams rather than assembled from multiple components. Each Uro-Cath® catheter has a thin, latex sheath section similar to a condom at one end—the part that is rolled over the head and shaft of the penis—and a heavier funnel-shaped, cup section at the other—where urine is drained from into a bag or other collection device—making them virtually “twist-proof” by their unique design. Uro-Cath® catheters range in size from 25mm, our smallest, to 40mm, our largest in 5mm increments to suit a variety of individual requirements. They are packaged individually in a window pouch allowing for quick, easy product identification without opening the pouch. The back side of the pouch contains detailed, illustrated, application instructions relative to the product purchased Contains: 1 Uro-Cath® Male External Catheter, 1 Urofoam®-2 Double-Sided Adhesive Foam Strip, Illustrated, application instructions on back of pouch/package FDA UDI
Identifiers
- Catalog Number
- 522140 FDA UDI
- Primary DI / UDI-DI
- 00792293221407 FDA UDI
- FDA Product Code
- NNX FDA UDI
- GMDN Term
- Urinary incontinence penis sheath/port, single-use FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 876.5250 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
Yes
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 40 Millimeter FDA UDIWeight — 0.018 Pound FDA UDI
Category: Urinary incontinence penis sheath/port, single-use
Uro-Cath® Molded-Latex Male External Catheter, Extra-Large 40mm with Urofoam®-2 by Urocare Products, Inc. — Class I — FDA UDI — listed in FDA GUDID
Similar devices
Also classified as Urinary incontinence penis sheath/port, single-use.
- Wideband™ Self-Adhering Male External Catheter — C. R. Bard, Inc. · Class I
- UltraFlex™ Self-Adhering Male External Catheter — C. R. Bard, Inc. · Class I
- LHB Industries — The Lighthouse For the Blind, Inc. · Class I
- SureStep Male External Catheter System Green Replacement Kit — C. R. Bard, Inc. · Class I
- Clear Advantage Male Continence Sheath — C. R. Bard, Inc. · Class I
- Wideband Male External Catheter — C. R. Bard, Inc. · Class I
- LHB Industries — The Lighthouse For the Blind, Inc. · Class I
- Spirit® Hydrocolloid Adhesive Sheath — C. R. Bard, Inc. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Urocare Products, Inc.
Sources (1)
- FDA UDI 017cd779-b5e4-4ac6-b0b9-e22f1a6cc7a4 36 fields · synced Jun 8, 2026