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extriCARE

FDA UDI

Class II (US FDA UDI)

by Oakwell Distribution, Inc.

Identity

Trade Name
extriCARE FDA UDI
Generic Name
Multi-purpose low-vacuum suction system FDA UDI
Device Name
NPWT Bandage-Foot with tubing set FDA UDI
Model / Reference
EC2400-F FDA UDI
Description
NPWT Bandage-Foot with tubing set FDA UDI

Identifiers

Primary DI / UDI-DI
00879766005631 FDA UDI
510(k) Number
K131464 FDA UDI
FDA Product Code
OMP FDA UDI
GMDN Term
Multi-purpose low-vacuum suction system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4780 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

Yes

FDA UDI

Category: Multi-purpose low-vacuum suction system

extriCARE by Oakwell Distribution, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-purpose low-vacuum suction system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Oakwell Distribution, Inc.

Sources (1)

  • FDA UDI 0d986a0f-a44e-49d2-9bc9-6f7f13acc55d 34 fields · synced May 30, 2026