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Acrodose PL System

FDA UDI

Class II (US FDA UDI)

by Haemonetics Corporation

Identity

Trade Name
Acrodose PL System FDA UDI
Generic Name
Blood/tissue storage/culture container FDA UDI
Device Name
Platelet Pool and Store Set with eBDS FDA UDI
Model / Reference
732-80 FDA UDI
Description
Platelet Pool and Store Set with eBDS FDA UDI

Identifiers

Primary DI / UDI-DI
10887691307888 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 PL 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Haemonetics Corporation

Sources (1)

  • FDA UDI fc9b4254-c108-4d32-8d4c-17a30d9ba08a 36 fields · synced Jun 8, 2026