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BD Copan FLOQSwabs for HPV Self Collection

FDA UDI

Class III (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Copan FLOQSwabs for HPV Self Collection FDA UDI
Generic Name
Urogenital specimen collection kit IVD, clinical FDA UDI
Device Name
BD Copan FLOQSwabs for HPV Self Collection FDA UDI
Model / Reference
445436 FDA UDI
Description
BD Copan FLOQSwabs for HPV Self Collection FDA UDI

Identifiers

Catalog Number
445436 FDA UDI
Primary DI / UDI-DI
30382904454365 FDA UDI
PMA Number
P160037 FDA UDI
FDA Product Code
MAQ FDA UDI
GMDN Term
Urogenital specimen collection kit IVD, clinical FDA UDI

Classification

Device Class
Class III FDA UDI
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

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

Category: Urogenital specimen collection kit IVD, clinical

BD Copan FLOQSwabs for HPV Self Collection by Becton Dickinson And Company — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Urogenital specimen collection kit IVD, clinical.

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 08e0da71-fce8-4984-a120-7e938ab47c94 37 fields · synced May 31, 2026