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BD ProbeTec™ ET Instrument, Remanufactured

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD ProbeTec™ ET Instrument, Remanufactured FDA UDI
Generic Name
Thermal cycler nucleic acid amplification analyser IVD, laboratory FDA UDI
Device Name
BD ProbeTec™ ET Instrument, Remanufactured FDA UDI
Model / Reference
440716 FDA UDI
Description
BD ProbeTec™ ET Instrument, Remanufactured FDA UDI

Identifiers

Catalog Number
440716 FDA UDI
Primary DI / UDI-DI
00382904407162 FDA UDI
FDA Product Code
LSL FDA UDI
GMDN Term
Thermal cycler nucleic acid amplification analyser IVD, laboratory 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

No

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Depth — 28.5 Inch FDA UDI
Width — 28.5 Inch FDA UDI
Height — 21.5 Inch FDA UDI

BD ProbeTec™ ET Instrument, Remanufactured by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 82e12876-14fa-4f48-b6c4-d6fd9f9b638b 38 fields · synced May 30, 2026