← Back to catalogue

SurePath Preservative Fluid Collection Vial

FDA UDI

Class III (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
SurePath Preservative Fluid Collection Vial FDA UDI
Generic Name
Cytology specimen container IVD, transport buffer FDA UDI
Device Name
SurePath® GYN Preservative Vial Kit: 10 mL SurePath® Preservative Fluid Collection Vials (500) FDA UDI
Model / Reference
490527 FDA UDI
Description
SurePath® GYN Preservative Vial Kit: 10 mL SurePath® Preservative Fluid Collection Vials (500) FDA UDI

Identifiers

Catalog Number
490527 FDA UDI
Primary DI / UDI-DI
10382904905276 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
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

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

Dimensions & Sizes

Size
Width — 44.2 Centimeter FDA UDI
Length — 44.2 Centimeter FDA UDI
Height — 8.3 Centimeter FDA UDI

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

Cleared under the same submission

P970018 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Becton Dickinson And Company

Sources (1)

  • FDA UDI 50727383-baaf-4989-b37b-20ddaef70346 39 fields · synced May 30, 2026