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Rovers® Cervex-Brush®

FDA UDI

Class II (US FDA UDI)

by Rovers Medical Devices B.V.

Identity

Trade Name
Rovers® Cervex-Brush® FDA UDI
Generic Name
Cytology scraper, single-use FDA UDI
Device Name
The Cervex-Brush® is a single-use cell sampler intended to collect simultaneous cell material from the cervical os, ectocervical and endo cervical canal in women. FDA UDI
Model / Reference
380300331 FDA UDI
Description
The Cervex-Brush® is a single-use cell sampler intended to collect simultaneous cell material from the cervical os, ectocervical and endo cervical canal in women. FDA UDI

Identifiers

Primary DI / UDI-DI
18719189246398 FDA UDI
510(k) Number
K930955 FDA UDI
FDA Product Code
HHT FDA UDI
GMDN Term
Cytology scraper, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4530 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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: Cytology scraper, single-use

Rovers® Cervex-Brush® by Rovers Medical Devices B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cytology scraper, single-use.

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 2bd720bd-4072-41f3-b719-05ad0060137f 34 fields · synced May 30, 2026