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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
Suction system catheter, general-purpose FDA UDI
Device Name
Cardiac Sucker, flexible, fluted tip, 1/4" connector, 14.5" length, non-sterile FDA UDI
Model / Reference
SUC-0840 FDA UDI
Description
Cardiac Sucker, flexible, fluted tip, 1/4" connector, 14.5" length, non-sterile FDA UDI

Identifiers

Catalog Number
SUC-0840 FDA UDI
Primary DI / UDI-DI
00817278012495 FDA UDI
FDA Product Code
GCX FDA UDI
GMDN Term
Suction system catheter, general-purpose FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Suction system catheter, general-purpose

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

Similar devices

Also classified as Suction system catheter, general-purpose.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI de59c42a-1dd9-48e4-935f-0b9a51fa9b21 34 fields · synced Jun 8, 2026