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Blood Gas blood collection capillary tubes

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Blood Gas blood collection capillary tubes FDA UDI
Generic Name
Capillary blood collection tube IVD, lithium heparin FDA UDI
Device Name
100 blood collection capillary tubes. Each tube contains 130-200 units/mL Lithium Heparin (approx. volume 100µL) FDA UDI
Model / Reference
10321712 FDA UDI
Description
100 blood collection capillary tubes. Each tube contains 130-200 units/mL Lithium Heparin (approx. volume 100µL) FDA UDI

Identifiers

Catalog Number
478600 FDA UDI
Primary DI / UDI-DI
00630414115740 FDA UDI
FDA Product Code
GIO FDA UDI
GMDN Term
Capillary blood collection tube IVD, lithium heparin 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Capillary blood collection tube IVD, lithium heparin

Blood Gas blood collection capillary tubes by Siemens Healthcare Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Capillary blood collection tube IVD, lithium heparin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 610be4d9-938f-4f77-b31d-27f3daaa4716 36 fields · synced May 31, 2026