← Back to catalogue
BD ProbeTec™ Trichomonas vaginalis (TV) Qx Amplified DNA Assay
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- BD ProbeTec™ Trichomonas vaginalis (TV) Qx Amplified DNA Assay FDA UDI
- Generic Name
- Trichomonas vaginalis nucleic acid IVD, kit, nucleic acid technique (NAT) FDA UDI
- Device Name
- BD ProbeTec™ Trichomonas vaginalis (TV) Qx Amplified DNA Assay FDA UDI
- Model / Reference
- 441917 FDA UDI
- Description
- BD ProbeTec™ Trichomonas vaginalis (TV) Qx Amplified DNA Assay FDA UDI
Identifiers
- Catalog Number
- 441917 FDA UDI
- Primary DI / UDI-DI
- 00382904419172 FDA UDI
- 510(k) Number
- K130268 FDA UDI
- FDA Product Code
- OUY FDA UDI
- GMDN Term
- Trichomonas vaginalis nucleic acid IVD, kit, nucleic acid technique (NAT) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.3860 FDA UDI
- 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
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
BD ProbeTec™ Trichomonas vaginalis (TV) Qx Amplified DNA Assay by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Becton Dickinson And Company
Sources (1)
- FDA UDI 11b734bd-e9da-4846-94fe-dbc78ea505e1 38 fields · synced Jun 1, 2026