← Back to catalogue

Valve Module (unheated)

FDA UDI

Class II (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Valve Module (unheated) FDA UDI
Generic Name
Blood gas/haemoximetry analyser IVD, point-of-care FDA UDI
Device Name
Valve module an in vitro diagnostics device to be used on the RAPIDChem® 744/754 analyzer FDA UDI
Model / Reference
10309056 FDA UDI
Description
Valve module an in vitro diagnostics device to be used on the RAPIDChem® 744/754 analyzer FDA UDI

Identifiers

Catalog Number
3372381 FDA UDI
Primary DI / UDI-DI
00630414452142 FDA UDI
510(k) Number
K000926 FDA UDI
FDA Product Code
CEM FDA UDI
CGZ FDA UDI
JGS FDA UDI
GMDN Term
Blood gas/haemoximetry analyser IVD, point-of-care FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1600 FDA UDI
862.1170 FDA UDI
862.1665 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Blood gas/haemoximetry analyser IVD, point-of-care

Valve Module (unheated) by Siemens Healthcare Diagnostics — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood gas/haemoximetry analyser IVD, point-of-care.

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 55ddbd39-3355-4187-a850-c109e215885e 36 fields · synced May 29, 2026