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Surge Casrdiovascular

FDA UDI

Class I (US FDA UDI)

by Med Michigan Holdings Llc

Identity

Trade Name
Surge Casrdiovascular FDA UDI
Generic Name
Cardiopulmonary bypass cannula holder set FDA UDI
Device Name
Complete Adult Tourniquet Kit with Snare, 1 red, 1 blue, 3 clear, 7" length, non-sterile FDA UDI
Model / Reference
TOU-7906 FDA UDI
Description
Complete Adult Tourniquet Kit with Snare, 1 red, 1 blue, 3 clear, 7" length, non-sterile FDA UDI

Identifiers

Catalog Number
TOU-7906 FDA UDI
Primary DI / UDI-DI
00817278011313 FDA UDI
FDA Product Code
GDJ FDA UDI
GMDN Term
Cardiopulmonary bypass cannula holder set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

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: Cardiopulmonary bypass cannula holder set

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

Similar devices

Also classified as Cardiopulmonary bypass cannula holder set.

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 8a4050d2-4fc1-41f4-873e-af9fddf078e1 34 fields · synced May 30, 2026