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QUADROX-i

FDA UDI

Class II (US FDA UDI)

by Maquet Cardiopulmonary AG

Identity

Trade Name
QUADROX-i FDA UDI
Generic Name
Extracorporeal membrane oxygenator FDA UDI
Device Name
QUADROX-i Small Adult Microporous Membrane Oxygenator with integrated arterial filter, BIOLINE coated, with a screw connector FDA UDI
Model / Reference
BEQ-HMO 51000 #SQUADR-i Small Adult +Fi. / Small Adult, Filter; BIOLINE Coating FDA UDI
Description
QUADROX-i Small Adult Microporous Membrane Oxygenator with integrated arterial filter, BIOLINE coated, with a screw connector FDA UDI

Identifiers

Catalog Number
70106.7911 FDA UDI
Primary DI / UDI-DI
04058863019178 FDA UDI
510(k) Number
K150267 FDA UDI
FDA Product Code
DTZ FDA UDI
DTM FDA UDI
DTR FDA UDI
GMDN Term
Extracorporeal membrane oxygenator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4350 FDA UDI
870.4260 FDA UDI
870.4240 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

Yes

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
Total Volume — 295 Milliliter FDA UDI

QUADROX-i by Maquet Cardiopulmonary AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K150267 also covers:

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 4d166c65-597f-4244-b082-727cd7d18790 38 fields · synced May 30, 2026