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ThinPrep Pap Test

FDA UDI

Class III (US FDA UDI)

by Hologic, Inc.

Identity

Trade Name
ThinPrep Pap Test FDA UDI
Generic Name
Cervical cytology microscopy slide IVD FDA UDI
Device Name
Glass slides for use with ThinPrep® processors for gynecological specimens. FDA UDI
Model / Reference
ThinPrep® Pap Test Microscope Slides, 100pk FDA UDI
Description
Glass slides for use with ThinPrep® processors for gynecological specimens. FDA UDI

Identifiers

Catalog Number
70373-001 FDA UDI
Primary DI / UDI-DI
25420045501109 FDA UDI
PMA Number
P950039 FDA UDI
FDA Product Code
MKQ FDA UDI
GMDN Term
Cervical cytology microscopy slide IVD 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cervical cytology microscopy slide IVD

ThinPrep Pap Test by Hologic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cervical cytology microscopy slide IVD.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hologic, Inc.

Sources (1)

  • FDA UDI 398dee87-cda2-4a45-991c-1a936743e328 36 fields · synced May 29, 2026