Identity
- Trade Name
- RhinoCath Nasal Suction FDA UDI
- Generic Name
- Nasal haemostatic catheter FDA UDI
- Model / Reference
- SP-45000 FDA UDI
Identifiers
- Catalog Number
- SP-45000 FDA UDI
- Primary DI / UDI-DI
- 00385640000093 FDA UDI
- FDA Product Code
- GCY FDA UDI
- GMDN Term
- Nasal haemostatic catheter FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 878.4680 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
No
FDA UDI
Category: Nasal haemostatic catheter
RhinoCath Nasal Suction by Summit Medical, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Nasal haemostatic catheter.
- Nasal Sponges Sterile — Dynarex Corp. · 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
- Summit Medical, LLC
Sources (1)
- FDA UDI b95fa713-1b2d-4ee1-980e-2a1686debc3e 34 fields · synced Jun 6, 2026