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Ready Sensor™ Glucose Biosensor

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Ready Sensor™ Glucose Biosensor FDA UDI
Generic Name
Laboratory pH electrode FDA UDI
Device Name
In vitro diagnostics medical device. For measurement of glucose in Siemens Healthcare Diagnostics RAPIDLab® Series systems. FDA UDI
Model / Reference
10320748 FDA UDI
Description
In vitro diagnostics medical device. For measurement of glucose in Siemens Healthcare Diagnostics RAPIDLab® Series systems. FDA UDI

Identifiers

Catalog Number
476378 FDA UDI
Primary DI / UDI-DI
00630414112343 FDA UDI
510(k) Number
K934907 FDA UDI
FDA Product Code
CHL FDA UDI
GMDN Term
Laboratory pH electrode FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1120 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

No

FDA UDI

Category: Laboratory pH electrode

Ready Sensor™ Glucose Biosensor by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laboratory pH electrode.

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 94d24c46-2cbc-41fe-b9fb-f9cf8c62fe6f 37 fields · synced Jun 6, 2026