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CPM Dx

FDA UDI

Class I (US FDA UDI)

by Agena Bioscience, Inc.

Identity

Trade Name
CPM Dx FDA UDI
Generic Name
Laboratory liquid dispenser, electronic FDA UDI
Model / Reference
31245 FDA UDI

Identifiers

Catalog Number
31245 FDA UDI
Primary DI / UDI-DI
00850010566016 FDA UDI
FDA Product Code
DOP FDA UDI
GMDN Term
Laboratory liquid dispenser, electronic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2860 FDA UDI
Commercial Distribution
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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Laboratory liquid dispenser, electronic

CPM Dx by Agena Bioscience, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laboratory liquid dispenser, electronic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4f20c1c8-a5ea-41c4-8577-d9e7cb203f2d 34 fields · synced May 30, 2026