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Epiflo®

FDA UDI

Class II (US FDA UDI)

by Ogenix

Identity

Trade Name
EPIFLO® FDA UDI
Generic Name
Wound therapy oxygenator, single-use FDA UDI
Device Name
Transdermal Continuous O2 Therapy Oxygen Concentrator and 6 Cannulas FDA UDI
Model / Reference
28-day FDA UDI
Description
Transdermal Continuous O2 Therapy Oxygen Concentrator and 6 Cannulas FDA UDI

Identifiers

Catalog Number
01-130-100010 FDA UDI
Primary DI / UDI-DI
00855526003079 FDA UDI
510(k) Number
K190742 FDA UDI
FDA Product Code
KPJ FDA UDI
GMDN Term
Wound therapy oxygenator, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5650 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Wound therapy oxygenator, single-use

Epiflo® by Ogenix — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wound therapy oxygenator, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ogenix

Sources (1)

  • FDA UDI 14a75319-35d1-4a1f-b934-a6ca2932ad23 36 fields · synced May 31, 2026