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Phoenix Diagnostics, Inc.

FDA UDI

Class II (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
Rinse Solution for I.L. 943 FDA UDI
Model / Reference
13-020 FDA UDI
Description
Rinse Solution for I.L. 943 FDA UDI

Identifiers

Primary DI / UDI-DI
00853366007714 FDA UDI
FDA Product Code
JIX FDA UDI
GMDN Term
Wash/cleaning solution IVD, automated/semi-automated system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1150 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 II — 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

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Manufacturer

Sources (1)

  • FDA UDI c2337525-faae-4c77-99e8-c2d7477130ef 33 fields · synced Jun 6, 2026