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MPS® Mini-Prime Delivery Set

FDA UDI

Class II (US FDA UDI)

by Quest Medical Inc

Identity

Trade Name
MPS® Mini-Prime Delivery Set FDA UDI
Generic Name
Cardioplegia solution administration kit FDA UDI
Device Name
MPS® Mini-Prime Delivery Set with Arrest and Additive Cassettes FDA UDI
Model / Reference
7001101 FDA UDI
Description
MPS® Mini-Prime Delivery Set with Arrest and Additive Cassettes FDA UDI

Identifiers

Primary DI / UDI-DI
00634624701113 FDA UDI
510(k) Number
K953838 FDA UDI
FDA Product Code
DTR FDA UDI
GMDN Term
Cardioplegia solution administration kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4240 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

Yes

FDA UDI

Category: Cardioplegia solution administration kit

MPS® Mini-Prime Delivery Set by Quest Medical Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardioplegia solution administration kit.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Quest Medical Inc

Sources (1)

  • FDA UDI 043efd1f-b4f2-4249-86ea-6091f0ed3276 34 fields · synced May 30, 2026