Identity
- Trade Name
- UK, Rapid Infuser, 230 V, 1000ml/min FDA UDI
- Generic Name
- Warming/high-flow infusion pump FDA UDI
- Model / Reference
- 903-00024-UK FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00896128002411 FDA UDI
- 510(k) Number
- K091855 FDA UDI
- FDA Product Code
- FRN FDA UDILGZ FDA UDI
- GMDN Term
- Warming/high-flow infusion pump FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5725 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
UK, Rapid Infuser, 230 V, 1000ml/min by Belmont Instrument Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
K091855 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Belmont Instrument Corp.
Sources (1)
- FDA UDI 0dcbae83-7fa8-4825-9a02-e7c55da2d5bf 34 fields · synced Jun 8, 2026