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WoundPro Outer Drape,

FDA UDI

Class II (US FDA UDI)

by Pensar Medical, LLC

Identity

Trade Name
WoundPro Outer Drape, FDA UDI
Generic Name
Negative-pressure wound therapy system drape FDA UDI
Device Name
WoundPro Outer Drape 2 per package (10 packages per box) FDA UDI
Model / Reference
8463540 0802 FDA UDI
Description
WoundPro Outer Drape 2 per package (10 packages per box) FDA UDI

Identifiers

Primary DI / UDI-DI
20851978007379 FDA UDI
510(k) Number
K150960 FDA UDI
FDA Product Code
OMP FDA UDI
GMDN Term
Negative-pressure wound therapy system drape 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: Negative-pressure wound therapy system drape

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

Similar devices

Also classified as Negative-pressure wound therapy system drape.

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 9609daff-b25b-49ea-ab48-9ec55ea6fb58 34 fields · synced May 30, 2026