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Luer Capillary

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Luer Capillary FDA UDI
Generic Name
Multiple blood gas/haemoximetry/electrolyte analyte IVD, reagent FDA UDI
Device Name
Luer Capillary (pack of 20) an in vitro diagnostics device for use on the RAPIDLab® 1200 series analyzers. FDA UDI
Model / Reference
10309073 FDA UDI
Description
Luer Capillary (pack of 20) an in vitro diagnostics device for use on the RAPIDLab® 1200 series analyzers. FDA UDI

Identifiers

Catalog Number
4142460 FDA UDI
Primary DI / UDI-DI
00630414482361 FDA UDI
FDA Product Code
GIO FDA UDI
GMDN Term
Multiple blood gas/haemoximetry/electrolyte analyte IVD, reagent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.6150 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multiple blood gas/haemoximetry/electrolyte analyte IVD, reagent

Luer Capillary by Siemens Healthcare Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multiple blood gas/haemoximetry/electrolyte analyte IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Siemens Healthcare Diagnostics

Sources (1)

  • FDA UDI 01900242-ea74-4063-b3ca-59b08ee45ea9 35 fields · synced May 30, 2026