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ADVIA® Chemistry Systems Reference Electrode

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
ADVIA® Chemistry Systems Reference Electrode FDA UDI
Generic Name
Reference electrode IVD FDA UDI
Device Name
ISE Reference Electrode - ADVIA Chem. - CONS - 1 Piece FDA UDI
Model / Reference
10309465 FDA UDI
Description
ISE Reference Electrode - ADVIA Chem. - CONS - 1 Piece FDA UDI

Identifiers

Catalog Number
073-0653-01 FDA UDI
Primary DI / UDI-DI
00630414478654 FDA UDI
510(k) Number
K990346 FDA UDI
FDA Product Code
JJE FDA UDI
GMDN Term
Reference electrode IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.2160 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Reference electrode IVD

ADVIA® Chemistry Systems Reference Electrode by Siemens Healthcare Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Reference electrode IVD.

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 aa6a291c-6bab-45b2-b79f-c37e617c79b7 36 fields · synced May 31, 2026