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ThinPrep 3000 Processor

FDA UDI

Class III (US FDA UDI)

by Hologic, Inc.

Identity

Trade Name
ThinPrep 3000 Processor FDA UDI
Generic Name
Microscope slide maker IVD FDA UDI
Device Name
Processes liquid based cytologic specimens to produce a uniform layer of cells on a glass microsope slide. FDA UDI
Model / Reference
ThinPrep 3000 Processor FDA UDI
Description
Processes liquid based cytologic specimens to produce a uniform layer of cells on a glass microsope slide. FDA UDI

Identifiers

Catalog Number
70150-001 FDA UDI
Primary DI / UDI-DI
15420045500846 FDA UDI
PMA Number
P950039 FDA UDI
FDA Product Code
MKQ FDA UDI
GMDN Term
Microscope slide maker IVD 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

ThinPrep 3000 Processor by Hologic, Inc. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

P950039 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hologic, Inc.

Sources (1)

  • FDA UDI bd7fc24e-e1b5-4992-b02b-c9a58522ca65 38 fields · synced May 30, 2026