← Back to catalogue

Phoenix Diagnostics, Inc.

FDA UDI

Class I (US FDA UDI)

by Phoenix Diagnostics, Inc.

Identity

Trade Name
PHOENIX DIAGNOSTICS, INC. FDA UDI
Generic Name
Wash/cleaning solution IVD, automated/semi-automated system FDA UDI
Device Name
Wash Solution for Olympus AU Series Chemistry Systems FDA UDI
Model / Reference
21-110 FDA UDI
Description
Wash Solution for Olympus AU Series Chemistry Systems FDA UDI

Identifiers

Primary DI / UDI-DI
00853366007745 FDA UDI
FDA Product Code
JCB FDA UDI
GMDN Term
Wash/cleaning solution IVD, automated/semi-automated system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4010 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wash/cleaning solution IVD, automated/semi-automated system

Phoenix Diagnostics, Inc. by Phoenix Diagnostics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wash/cleaning solution IVD, automated/semi-automated system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI a6d5713d-dfdd-4164-aa40-09cf1cebccbf 33 fields · synced Jun 1, 2026