Identity
- Trade Name
- Fluido® Compact FDA UDI
- Generic Name
- Conduction blood/fluid warmer FDA UDI
- Device Name
- Fluido® Compact Control Module FDA UDI
- Model / Reference
- Control Module FDA UDI
- Description
- Fluido® Compact Control Module FDA UDI
Identifiers
- Catalog Number
- 650100-US FDA UDI
- Primary DI / UDI-DI
- 18719867002421 FDA UDI
- 510(k) Number
- K211618 FDA UDI
- FDA Product Code
- LGZ FDA UDI
- GMDN Term
- Conduction blood/fluid warmer FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5725 FDA UDI
- Commercial Distribution
- 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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Conduction blood/fluid warmer
Fluido® Compact by The Surgical Company International B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- The Surgical Company International B.V.
Sources (1)
- FDA UDI 80e5a36e-428c-4180-b12b-493b2c3578b4 35 fields · synced Jun 1, 2026