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Hemo-Tap

FDA UDI

Class II (US FDA UDI)

by Utah Medical Products, Inc.

Identity

Trade Name
HEMO-TAP FDA UDI
Generic Name
Blood transfusion filter FDA UDI
Device Name
VALVE, Blood Bag Spike with StopCock FDA UDI
Model / Reference
Valve FDA UDI
Description
VALVE, Blood Bag Spike with StopCock FDA UDI

Identifiers

Catalog Number
4020609 FDA UDI
Primary DI / UDI-DI
H67140206090 FDA UDI
510(k) Number
K781815 FDA UDI
FDA Product Code
FPB FDA UDI
GMDN Term
Blood transfusion filter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5440 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

Category: Blood transfusion filter

Hemo-Tap by Utah Medical Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood transfusion filter.

Cleared under the same submission

K781815 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Utah Medical Products, Inc.

Sources (1)

  • FDA UDI 76686b1b-016f-4b72-92d6-5bd262fba275 36 fields · synced Jun 9, 2026