Identity
- Trade Name
- Goldberg FDA UDI
- Generic Name
- Urethral/suprapubic catheter valve-connector FDA UDI
- Device Name
- Goldberg Ureteral Adapter FDA UDI
- Model / Reference
- G15030 FDA UDI
- Description
- Goldberg Ureteral Adapter FDA UDI
Identifiers
- Catalog Number
- 050049 FDA UDI
- Primary DI / UDI-DI
- 00827002150300 FDA UDI
- FDA Product Code
- FCN FDA UDI
- GMDN Term
- Urethral/suprapubic catheter valve-connector FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5250 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
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
Category: Urethral/suprapubic catheter valve-connector
Goldberg by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Urethral/suprapubic catheter valve-connector.
- Bard® Ureteral Catheter Adapter — C. R. Bard, Inc. · Class II
- Bard® Flip-Flo™ Catheter Valve — C. R. Bard, Inc. · Class II
- Bard® Adapter and Tubing — C. R. Bard, Inc. · Class II
- BioFlo — INSERT MOLDING SOLUTIONS, INC. · Class II
- Bard® Flip-Flo™ Catheter Valve — C. R. Bard, Inc. · Class II
- Cook — COOK INCORPORATED · 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 II | Pending data |
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Manufacturer
- Manufacturer
- Cook Incorporated
Sources (1)
- FDA UDI 9eb34249-e6a3-450f-a780-f14534eec682 36 fields · synced Jun 8, 2026