Pop-On™ Self-Adhering Male External Catheter 32303
Ref 32303
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number0801741WJQSKQRHAQ 00801741070563 | Date10 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00801741070563 | Date27 Sep 2017 | StatusListed |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Pop-On EUDAMEDPop-On™ Self-Adhering Male External Catheter GUDID
- Generic Name
- Urinary incontinence penis sheath/port, single-use
- Model / Ref / Catalog
- 32303
- Primary DI / UDI-DI
- 00801741070563
- Basic UDI-DI
- 0801741WJQSKQRHAQ
- FDA Product Code
- NNX
- EMDN Code
- U070201 Sheath catheter for the treatment of incontinence
- GMDN Term
- Urinary incontinence penis sheath/port, single-use
- Device Class
- Class I
- Regulation Number
- 876.5250
- EU market of registration
- Belgium
- GUDID distribution status
- In Commercial Distribution
- Size
- Circumference — 32 Millimeter
Other devices from C. R. Bard, Inc.
Properties
Other properties (19)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Prescription Use: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Manufacturing Date: No