← Back to catalogue

DeRoyal

FDA UDI

Class I (US FDA UDI)

by Deroyal Industries, Inc.

Identity

Trade Name
DeRoyal FDA UDI
Generic Name
Negative-pressure wound therapy system dressing set FDA UDI
Device Name
Prospera PRO NPWT Kit w/ Prospera Propel Technology FDA UDI
Model / Reference
NP-6002P FDA UDI
Description
Prospera PRO NPWT Kit w/ Prospera Propel Technology FDA UDI

Identifiers

Catalog Number
NP-6002P FDA UDI
Primary DI / UDI-DI
00749756387743 FDA UDI
FDA Product Code
KDD FDA UDI
GMDN Term
Negative-pressure wound therapy system dressing set FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Negative-pressure wound therapy system dressing set

DeRoyal by Deroyal Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Negative-pressure wound therapy system dressing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI b1c39b11-2c7b-4579-b3ae-a92a8e81fa5b 35 fields · synced Jun 8, 2026