Identity
- Trade Name
- RAMP® NT-proBNP TEST KIT; 25 TESTS FDA UDI
- Generic Name
- B-type natriuretic protein/N-terminal pro b-type natriuretic peptide IVD, kit, rapid ICT, clinical FDA UDI
- Model / Reference
- C1105 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 10627966005046 FDA UDI
- GMDN Term
- B-type natriuretic protein/N-terminal pro b-type natriuretic peptide IVD, kit, rapid ICT, clinical FDA UDI
- Models / Variants
- RAMP® NT-proBNP 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: B-type natriuretic protein/N-terminal pro b-type natriuretic peptide IVD, kit, rapid ICT, clinical
RAMP® NT-proBNP TEST KIT +1 more model by Response Biomedical Corp — FDA UDI — listed in FDA GUDID — 2 models — regulatory data on deviCERTS
Similar devices
Also classified as B-type natriuretic protein/N-terminal pro b-type natriuretic peptide IVD, kit, rapid ICT, clinical.
- Nano-CheckTM 4 in 1 Test — Nano-Ditech Corporation · Class II
- Nano-CheckTM NT-proBNP — Nano-Ditech Corporation · Class II
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 6b3cecc2-5929-4629-88f2-94ec7f15e4fc 32 fields · synced May 30, 2026