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Elecsys tPSA

FDA UDI

Class III (US FDA UDI)

by Roche Diagnostics Corp.

Identity

Trade Name
Elecsys tPSA FDA UDI
Generic Name
Total prostate specific antigen (tPSA) IVD, kit, chemiluminescent immunoassay FDA UDI
Device Name
tPSA reagent, 100 Test-Kit FDA UDI
Model / Reference
04641655160 FDA UDI
Description
tPSA reagent, 100 Test-Kit FDA UDI

Identifiers

Catalog Number
04641655160 FDA UDI
Primary DI / UDI-DI
07613336154366 FDA UDI
PMA Number
P990056 FDA UDI
FDA Product Code
MTF FDA UDI
GMDN Term
Total prostate specific antigen (tPSA) IVD, kit, chemiluminescent immunoassay 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Total prostate specific antigen (tPSA) IVD, kit, chemiluminescent immunoassay

Elecsys tPSA by Roche Diagnostics Corp. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total prostate specific antigen (tPSA) IVD, kit, chemiluminescent immunoassay.

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 1128354f-f86f-43ce-ae36-18e78719f5cd 36 fields · synced Jun 1, 2026