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BD SurePath™ GYN Preservative Vial Kit with Brush/Spatula

FDA UDI

Class III (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD SurePath™ GYN Preservative Vial Kit with Brush/Spatula FDA UDI
Generic Name
Urogenital specimen collection kit IVD, clinical FDA UDI
Device Name
BD SurePath™ GYN Preservative Vial Kit with Brush/Spatula FDA UDI
Model / Reference
491440 FDA UDI
Description
BD SurePath™ GYN Preservative Vial Kit with Brush/Spatula FDA UDI

Identifiers

Catalog Number
491440 FDA UDI
Primary DI / UDI-DI
00382904914400 FDA UDI
PMA Number
P970018 FDA UDI
FDA Product Code
MKQ 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

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: Urogenital specimen collection kit IVD, clinical

BD SurePath™ GYN Preservative Vial Kit with Brush/Spatula by Becton Dickinson And Company — Class III — FDA UDI — listed in FDA GUDID

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 8574bd52-1f7f-4e0b-8927-f75e4b226e15 37 fields · synced May 30, 2026