← Back to catalogue

Phoenix Diagnostics, Inc.

FDA UDI

Class II (US FDA UDI)

by Phoenix Diagnostics, Inc.

Identity

Trade Name
PHOENIX DIAGNOSTICS, INC. FDA UDI
Generic Name
Chloride (Cl-) electrode IVD FDA UDI
Device Name
Cl- Electrode for Olympus AU Series Chemistry Systems FDA UDI
Model / Reference
E-920 FDA UDI
Description
Cl- Electrode for Olympus AU Series Chemistry Systems FDA UDI

Identifiers

Primary DI / UDI-DI
00853366007127 FDA UDI
510(k) Number
K020148 FDA UDI
FDA Product Code
CGZ FDA UDI
GMDN Term
Chloride (Cl-) electrode IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1170 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Chloride (Cl-) electrode IVD

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

Similar devices

Also classified as Chloride (Cl-) electrode IVD.

Cleared under the same submission

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 dd951cdd-848f-4e3a-badf-dca03f49e90d 34 fields · synced May 30, 2026