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Surge Cardiovascular

FDA UDI

Class II (US FDA UDI)

by Med Michigan Holdings Llc

Identity

Trade Name
Surge Cardiovascular FDA UDI
Generic Name
Cardioplegia solution administration adaptor FDA UDI
Device Name
Perfusion Cannula, one-way, 3mm blunt tip FDA UDI
Model / Reference
PER-3001S FDA UDI
Description
Perfusion Cannula, one-way, 3mm blunt tip FDA UDI

Identifiers

Catalog Number
PER-3001S FDA UDI
Primary DI / UDI-DI
00817278010378 FDA UDI
FDA Product Code
DWF FDA UDI
GMDN Term
Cardioplegia solution administration adaptor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4210 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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Cardioplegia solution administration adaptor

Surge Cardiovascular by Med Michigan Holdings Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cardioplegia solution administration adaptor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Med Michigan Holdings Llc

Sources (1)

  • FDA UDI 3da86119-389e-4fcf-ad39-b20905e9d4b4 34 fields · synced May 30, 2026