Identity
- Trade Name
- Salem Sump FDA UDI
- Generic Name
- Sump drain FDA UDI
- Device Name
- Silicone Dual Lumen Stomach Tube,Anti-Reflux Valve and Kangaroo CO2 Detector with Bellows FDA UDI
- Model / Reference
- 266130CN FDA UDI
- Description
- Silicone Dual Lumen Stomach Tube,Anti-Reflux Valve and Kangaroo CO2 Detector with Bellows FDA UDI
Identifiers
- Catalog Number
- 266130CN FDA UDI
- Primary DI / UDI-DI
- 10884521141292 FDA UDI
- FDA Product Code
- FEG FDA UDI
- GMDN Term
- Sump drain FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 876.5980 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
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Dimensions & Sizes
- Size
- Catheter Gauge — 16 French FDA UDI
Category: Sump drain
Salem Sump by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Sump drain.
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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
- Cardinalhealth
Sources (1)
- FDA UDI 8852da39-37b3-4702-bad8-09447d41ee95 37 fields · synced May 30, 2026