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Capiox®fx

FDA UDI

Class II (US FDA UDI)

by Terumo Corp.

Identity

Trade Name
CAPIOX®FX FDA UDI
Generic Name
Extracorporeal membrane oxygenator FDA UDI
Device Name
FX25 FDA UDI
Model / Reference
CX*FX25RW FDA UDI
Description
FX25 FDA UDI

Identifiers

Primary DI / UDI-DI
04987350701046 FDA UDI
FDA Product Code
DTZ FDA UDI
GMDN Term
Extracorporeal membrane oxygenator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4350 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

No

FDA UDI

Dimensions & Sizes

Size
Area/Surface Area — 2.5 Square meter FDA UDI

Category: Extracorporeal membrane oxygenator

Capiox®fx by Terumo Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Extracorporeal membrane oxygenator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Terumo Corp.

Sources (1)

  • FDA UDI 43ca5abf-476a-4ff1-bfa9-8535d714e8b8 36 fields · synced May 31, 2026