Glo-Tip Spray Catheter
Ref GT-7-SPRAY
Active
CE MDD 510(k)
Valid until
Not listed
FDA recalls
None foundTrust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-00827002248922 00827002248922 | Date27 Feb 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00827002248922 | Date30 Oct 2019 | StatusListed |
| United States | FDA 510(k) 510(k) | NumberK182319 | Date1 Feb 2019 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls found in the data synced 23 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- United States
- European Union
Specification
- Trade Name
- Glo-Tip
- Generic Name
- ERCP catheter, non-balloon, non-electrical, single-use
- Model / Ref / Catalog
- GT-7-SPRAY, G24892
- Primary DI / UDI-DI
- 00827002248922
- Basic UDI-DI
- B-00827002248922
- 510(k) Number
- FDA Product Code
- OCX
- EMDN Code
- G0304010199 Ercp cannulas, single-lumen - other
- GMDN Term
- ERCP catheter, non-balloon, non-electrical, single-use
- Device Class
- Class I EUDAMEDClass II GUDID
- Regulation Number
- 876.1500
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / Reference | GT-7-SPRAY | G24892 |
| Device Class | Class I | Class II |
Manufacturer details
- EUDAMED SRN
- US-MF-000002658
- Authorised representative
- COOK MEDICAL EUROPE LIMITED IE-AR-000000907
Other devices from Wilson-Cook Medical, Inc.
Properties
Other properties (16)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No