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Mcs+

FDA UDI

Class II (US FDA UDI)

by Haemonetics Corporation

Identity

Trade Name
MCS+ FDA UDI
Generic Name
Apheresis system FDA UDI
Device Name
MCS+ (RBC), LIST NO 08150-220-E FDA UDI
Model / Reference
08150-220-E FDA UDI
Description
MCS+ (RBC), LIST NO 08150-220-E FDA UDI

Identifiers

Primary DI / UDI-DI
30812747013851 FDA UDI
FDA Product Code
GKT FDA UDI
GMDN Term
Apheresis system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.9245 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: Apheresis system

Mcs+ by Haemonetics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Apheresis system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2e7bd371-af1d-4827-bab2-d733f4e6c86f 35 fields · synced Jun 8, 2026