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Haemonetics Mcs+ Apheresis System

FDA UDI

Class II (US FDA UDI)

by Haemonetics Corporation

Identity

Trade Name
HAEMONETICS MCS+ APHERESIS SYSTEM FDA UDI
Generic Name
Apheresis system tubing set FDA UDI
Device Name
MCS+ SDP/PLP W/SALINE,LN 994 FDA UDI
Model / Reference
00994-00 FDA UDI
Description
MCS+ SDP/PLP W/SALINE,LN 994 FDA UDI

Identifiers

Primary DI / UDI-DI
10812747012096 FDA UDI
FDA Product Code
GKT FDA UDI
GMDN Term
Apheresis system tubing set 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

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

Dimensions & Sizes

Size
Total Volume — 1000 Milliliter FDA UDI
Total Volume — 600 Milliliter FDA UDI
Total Volume — 50 Milliliter FDA UDI

Category: Apheresis system tubing set

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

Similar devices

Also classified as Apheresis system tubing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 896a8e75-2585-43e3-adb1-7a2af6f5e714 36 fields · synced Jun 8, 2026