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Capillary Caps

FDA UDI

Class I (US FDA UDI)

by Siemens Healthcare Diagnostics

Identity

Trade Name
Capillary Caps FDA UDI
Generic Name
Capillary blood collection tube IVD, electrolyte-balanced heparin FDA UDI
Device Name
200 capillary caps. An in vitro diagnostics medical device for use with Siemens Healthcare Diagnostics. 1.65mm OD Glass blood collection capillary tubes. FDA UDI
Model / Reference
10311053 FDA UDI
Description
200 capillary caps. An in vitro diagnostics medical device for use with Siemens Healthcare Diagnostics. 1.65mm OD Glass blood collection capillary tubes. FDA UDI

Identifiers

Catalog Number
478601 FDA UDI
Primary DI / UDI-DI
00630414115764 FDA UDI
FDA Product Code
GIO FDA UDI
GMDN Term
Capillary blood collection tube IVD, electrolyte-balanced 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Capillary blood collection tube IVD, electrolyte-balanced heparin

Capillary Caps 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, electrolyte-balanced heparin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 9055ab64-2354-4a4e-a76b-8797609b7043 35 fields · synced Jun 6, 2026