Identity
- Trade Name
- FloSense FDA UDI
- Generic Name
- Pulmonary function analysis system, adult FDA UDI
- Model / Reference
- Bidirectional kushion klip FDA UDI
Identifiers
- Catalog Number
- DP252-7 FDA UDI
- Primary DI / UDI-DI
- B279DP2527 FDA UDI
- 510(k) Number
- K990962 FDA UDI
- GMDN Term
- Pulmonary function analysis system, adult FDA UDI
Classification
- Commercial Distribution
- Not 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
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
FloSense by Sdi Diagnostics, Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Sdi Diagnostics, Inc.
Sources (1)
- FDA UDI 3ea79f55-36ea-4f64-bd54-45b24b7dda56 35 fields · synced May 30, 2026