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BD ProbeTec™ Chlamydia trachomatis (CT) Qx Amplified DNA Assay
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- BD ProbeTec™ Chlamydia trachomatis (CT) Qx Amplified DNA Assay FDA UDI
- Generic Name
- Chlamydia trachomatis nucleic acid IVD, kit, nucleic acid technique (NAT) FDA UDI
- Device Name
- Kit CT Qx Amplified Dna Assay FDA UDI
- Model / Reference
- 441126 FDA UDI
- Description
- Kit CT Qx Amplified Dna Assay FDA UDI
Identifiers
- Catalog Number
- 441126 FDA UDI
- Primary DI / UDI-DI
- 00382904411268 FDA UDI
- FDA Product Code
- LSL FDA UDIMKZ FDA UDI
- GMDN Term
- Chlamydia trachomatis nucleic acid IVD, kit, nucleic acid technique (NAT) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.3390 FDA UDI866.3120 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
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
BD ProbeTec™ Chlamydia trachomatis (CT) 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 |
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Manufacturer
- Manufacturer
- Becton Dickinson And Company
Sources (1)
- FDA UDI ab086da1-2fa1-4122-a70c-86164969ab94 38 fields · synced May 29, 2026