Identity
- Trade Name
- SAS Legionella Test FDA UDI
- Generic Name
- Legionella pneumophila antigen IVD, kit, rapid ICT, clinical FDA UDI
- Model / Reference
- 044020-M FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00780311000189 FDA UDI
- GMDN Term
- Legionella pneumophila antigen IVD, kit, rapid ICT, clinical FDA UDI
Classification
- Commercial Distribution
- 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
Yes
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Legionella pneumophila antigen IVD, kit, rapid ICT, clinical
SAS Legionella Test by Sa Scientific, Ltd — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Legionella pneumophila antigen IVD, kit, rapid ICT, clinical.
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Sa Scientific, Ltd
Sources (1)
- FDA UDI 3b35bcae-9d0d-48e0-9371-e6f4cac93658 32 fields · synced May 30, 2026