Identity
- Trade Name
- RAMP® RSV TEST KIT; 25 TESTS FDA UDI
- Generic Name
- Respiratory syncytial virus (RSV) antigen IVD, kit, fluorescent immunoassay FDA UDI
- Model / Reference
- C1108 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10627966005183 FDA UDI
- GMDN Term
- Respiratory syncytial virus (RSV) antigen IVD, kit, fluorescent immunoassay FDA UDI
- Models / Variants
- Ramp® Rsv Test Kit FDA UDI25 Tests 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Respiratory syncytial virus (RSV) antigen IVD, kit, fluorescent immunoassay
Ramp® Rsv Test Kit +1 more model by Response Biomedical Corp — FDA UDI — listed in FDA GUDID — 2 models — 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 | N/A | Pending data |
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Manufacturer
- Manufacturer
- Response Biomedical Corp
Sources (1)
- FDA UDI 3e46882b-3cae-4147-a5a9-6950ca2fcc2a 32 fields · synced May 31, 2026