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CBCII ConstaVac

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
CBCII ConstaVac FDA UDI
Generic Name
Whole-blood-recovery autotransfusion system, manual FDA UDI
Device Name
Blood Conservation Kit PVC w/o Fat Retention Valve FDA UDI
Model / Reference
0225414000S2 FDA UDI
Description
Blood Conservation Kit PVC w/o Fat Retention Valve FDA UDI

Identifiers

Catalog Number
0225-414-000S2 FDA UDI
Primary DI / UDI-DI
07613154585915 FDA UDI
FDA Product Code
CAC FDA UDI
GMDN Term
Whole-blood-recovery autotransfusion system, manual FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5830 FDA UDI
Commercial Distribution
Not 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

Yes

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

CBCII ConstaVac by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI ddcf0ef8-1486-4ca0-a9cb-13ded268e639 38 fields · synced Jun 1, 2026