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Whole Blood Collection and Transfusion Kit

FDA UDI

Class II (US FDA UDI)

by Altitude Technologies Inc.

Identity

Trade Name
Whole Blood Collection and Transfusion Kit FDA UDI
Generic Name
Blood transfusion set, non-exchange FDA UDI
Model / Reference
3425 FDA UDI

Identifiers

Primary DI / UDI-DI
00856767008083 FDA UDI
FDA Product Code
POQ FDA UDI
GMDN Term
Blood transfusion set, non-exchange 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

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: Blood transfusion set, non-exchange

Whole Blood Collection and Transfusion Kit by Altitude Technologies Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood transfusion set, non-exchange.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 50ca892d-27d5-4964-8943-043ee3cba3e0 32 fields · synced Jun 8, 2026