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Maquet Venous Return Catheter

FDA UDI

Class II (US FDA UDI)

by Maquet Cardiopulmonary AG

Identity

Trade Name
Maquet Venous Return Catheter FDA UDI
Generic Name
Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage FDA UDI
Device Name
Venous Return Catheter reinf. 36 F., straight, 9cm lumen-tip, sterile, no coating, single packed for clinical use. FDA UDI
Model / Reference
620369 FDA UDI
Description
Venous Return Catheter reinf. 36 F., straight, 9cm lumen-tip, sterile, no coating, single packed for clinical use. FDA UDI

Identifiers

Catalog Number
70102.3938 FDA UDI
Primary DI / UDI-DI
04037691237619 FDA UDI
510(k) Number
K872182 FDA UDI
FDA Product Code
DQY FDA UDI
GMDN Term
Cardiopulmonary bypass/extracorporeal membrane oxygenation cannula, drainage FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 FDA UDI
Commercial Distribution
Not 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

Dimensions & Sizes

Size
Weight — 90 Gram FDA UDI
Total Volume — 25 Liter FDA UDI
Length — 40 Centimeter FDA UDI
Catheter Gauge — 36 French FDA UDI

Maquet Venous Return Catheter by Maquet Cardiopulmonary AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Maquet Cardiopulmonary AG

Sources (1)

  • FDA UDI 2b186824-2016-453d-a52b-0734fb43080a 38 fields · synced May 30, 2026