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BD ProbeTec™ (GC) Qx Amplified DNA Assay

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD ProbeTec™ (GC) Qx Amplified DNA Assay FDA UDI
Generic Name
Neisseria gonorrhoeae nucleic acid IVD, kit, nucleic acid technique (NAT) FDA UDI
Device Name
Kit GC Qx Amplified Dna Assay FDA UDI
Model / Reference
441124 FDA UDI
Description
Kit GC Qx Amplified Dna Assay FDA UDI

Identifiers

Catalog Number
441124 FDA UDI
Primary DI / UDI-DI
00382904411244 FDA UDI
510(k) Number
K081825 FDA UDI
K090827 FDA UDI
K090971 FDA UDI
K091730 FDA UDI
FDA Product Code
LSL FDA UDI
GMDN Term
Neisseria gonorrhoeae nucleic acid IVD, kit, nucleic acid technique (NAT) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3390 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™ (GC) Qx Amplified DNA Assay by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ab92977d-55c3-47ef-9243-3cebb82715bb 38 fields · synced Jun 1, 2026