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Corvac

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Corvac FDA UDI
Generic Name
Non-evacuated blood collection tube IVD, no additive FDA UDI
Device Name
Integrated Serum Separator Tube,Red/Gray Stopper, 12.5 mL Draw FDA UDI
Model / Reference
8881302114 FDA UDI
Description
Integrated Serum Separator Tube,Red/Gray Stopper, 12.5 mL Draw FDA UDI

Identifiers

Catalog Number
8881302114 FDA UDI
Primary DI / UDI-DI
20884527003201 FDA UDI
FDA Product Code
GIM FDA UDI
GMDN Term
Non-evacuated blood collection tube IVD, no additive FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
862.1675 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Dimensions & Sizes

Size
Total Volume — 12.5 Milliliter FDA UDI
Length — 125 Millimeter FDA UDI
Outer Diameter — 16 Millimeter FDA UDI

Category: Non-evacuated blood collection tube IVD, no additive

Corvac by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Non-evacuated blood collection tube IVD, no additive.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI 54089b70-1595-4264-831f-36896e271cc6 37 fields · synced Jun 8, 2026