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BD SurePath™ Collection Vial

FDA UDI

Class III (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD SurePath™ Collection Vial FDA UDI
Generic Name
Cytology specimen container IVD, transport buffer FDA UDI
Device Name
BD SurePath™ Collection Vial FDA UDI
Model / Reference
491452 FDA UDI
Description
BD SurePath™ Collection Vial FDA UDI

Identifiers

Catalog Number
491452 FDA UDI
Primary DI / UDI-DI
10382904914520 FDA UDI
PMA Number
P970018 FDA UDI
FDA Product Code
MKQ FDA UDI
GMDN Term
Cytology specimen container IVD, transport buffer 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

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

Category: Cytology specimen container IVD, transport buffer

BD SurePath™ Collection Vial by Becton Dickinson And Company — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cytology specimen container IVD, transport buffer.

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 66f4d208-d266-4035-abb3-b477e2d61726 37 fields · synced May 30, 2026