Identity
- Trade Name
- moorFLPI-2 Clinical PC Software FDA UDI
- Generic Name
- Cutaneous microcirculation laser Doppler imaging device FDA UDI
- Device Name
- moorFLPI-2 Clinical PC Software V1 FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- moorFLPI-2 Clinical PC Software V1 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 15060484490157 FDA UDI
- 510(k) Number
- K122943 FDA UDI
- FDA Product Code
- DPT FDA UDI
- GMDN Term
- Cutaneous microcirculation laser Doppler imaging device FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2120 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
moorFLPI-2 Clinical PC Software by Moor Instruments Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Cleared under the same submission
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
- Moor Instruments Limited
Sources (1)
- FDA UDI 47fad94a-8e96-4962-aff4-d5d73e7b05d4 36 fields · synced Jun 1, 2026