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Haemonetics Cell Saver 5+ System

FDA UDI

Class II (US FDA UDI)

by Haemonetics Corporation

Identity

Trade Name
HAEMONETICS CELL SAVER 5+ SYSTEM FDA UDI
Generic Name
Autotransfusion system blood collection/processing pump FDA UDI
Device Name
CS5+,110V ENG, LN02005-110-EP FDA UDI
Model / Reference
02005-110-EP FDA UDI
Description
CS5+,110V ENG, LN02005-110-EP FDA UDI

Identifiers

Primary DI / UDI-DI
30812747016814 FDA UDI
510(k) Number
K932890 FDA UDI
FDA Product Code
CAC FDA UDI
GMDN Term
Autotransfusion system blood collection/processing pump FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5830 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Autotransfusion system blood collection/processing pump

Haemonetics Cell Saver 5+ System by Haemonetics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Autotransfusion system blood collection/processing pump.

Cleared under the same submission

K932890 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Haemonetics Corporation

Sources (1)

  • FDA UDI 9a009ce5-5e11-42cf-80bf-8f7d29e455b2 35 fields · synced Jun 8, 2026