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BD Blood Pump transfusion set

FDA UDIEUDAMED

Class II (US FDA UDI)

by Amsino International, Inc.

Identity

Trade Name
BD Blood Pump transfusion set FDA UDI
Generic Name
Blood transfusion set, non-exchange FDA UDI
Device Name
Blood Transfusion Set FDA UDI
Model / Reference
1 FDA UDI
Description
Blood Transfusion Set FDA UDI

Identifiers

Catalog Number
AM-TS-000 FDA UDI
Primary DI / UDI-DI
00704411011852 FDA UDI
510(k) Number
K983559 FDA UDI
FDA Product Code
FJK FDA UDI
GMDN Term
Blood transfusion set, non-exchange FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5820 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 set, non-exchange

BD Blood Pump transfusion set by Amsino International, Inc. — Class II — MDD, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Blood transfusion set, non-exchange.

Cleared under the same submission

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDD

United States Pending data

FDA UDI

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Manufacturer

Sources (2)

  • FDA UDI 75c60092-99ac-4b75-97c9-e639b03ae6eb 35 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced Jun 14, 2026