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WoundPro UniFlow Connector

FDA UDI

Class II (US FDA UDI)

by Pensar Medical, LLC

Identity

Trade Name
WoundPro UniFlow Connector FDA UDI
Generic Name
Low-pressure tubing connector, single-use, non-sterile FDA UDI
Device Name
WoundPro UniFlow Y Connector Case of 10 FDA UDI
Model / Reference
8463540 0674 FDA UDI
Description
WoundPro UniFlow Y Connector Case of 10 FDA UDI

Identifiers

Primary DI / UDI-DI
10851978007082 FDA UDI
510(k) Number
K150960 FDA UDI
FDA Product Code
OMP FDA UDI
GMDN Term
Low-pressure tubing connector, single-use, non-sterile 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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Low-pressure tubing connector, single-use, non-sterile

WoundPro UniFlow Connector by Pensar Medical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Low-pressure tubing connector, single-use, non-sterile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pensar Medical, LLC

Sources (1)

  • FDA UDI 666f0885-e362-4d39-8267-44d2425da52e 34 fields · synced Jun 8, 2026