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Ready Sensor™ GOLD pO2 Sensor

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Ready Sensor™ GOLD pO2 Sensor FDA UDI
Generic Name
Blood oxygen electrode IVD FDA UDI
Device Name
Ready Sensor™ pO2 Biosensor for use on the RapidLab® 248/348/348ex instruments FDA UDI
Model / Reference
10324408 FDA UDI
Description
Ready Sensor™ pO2 Biosensor for use on the RapidLab® 248/348/348ex instruments FDA UDI

Identifiers

Catalog Number
476246 FDA UDI
Primary DI / UDI-DI
00630414112077 FDA UDI
510(k) Number
K935830 FDA UDI
FDA Product Code
CHL FDA UDI
GMDN Term
Blood oxygen electrode IVD 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood oxygen electrode IVD

Ready Sensor™ GOLD pO2 Sensor by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood oxygen 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 dc01b64e-0737-475d-aa09-f8c7364c9b84 37 fields · synced May 30, 2026