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Acrodose PLus System

FDA UDI

Class II (US FDA UDI)

by Haemonetics Corporation

Identity

Trade Name
Acrodose PLus System FDA UDI
Generic Name
Blood/tissue storage/culture container FDA UDI
Device Name
Platelet Pool and Store Set with In-line Leukocyte Redcution Filter FDA UDI
Model / Reference
732-83 FDA UDI
Description
Platelet Pool and Store Set with In-line Leukocyte Redcution Filter FDA UDI

Identifiers

Primary DI / UDI-DI
10887691310697 FDA UDI
FDA Product Code
KSR FDA UDI
GMDN Term
Blood/tissue storage/culture container FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9100 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/tissue storage/culture container

Acrodose PLus System by Haemonetics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood/tissue storage/culture container.

Cleared under the same submission

BK080003 also covers:

BK090007 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 02e5a01c-c8a3-41e4-9b58-06bd9904ad28 35 fields · synced Jun 8, 2026