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Wound Free

FDA UDI

Class I (US FDA UDI)

by Applied Dental, Inc.

Identity

Trade Name
Wound Free FDA UDI
Generic Name
Waterproof skin adhesive tape FDA UDI
Device Name
IV Transparent Film Dressing, 6x7cm (2.375" x 2.75"). Sterile. FDA UDI
Model / Reference
WIV-0607 FDA UDI
Description
IV Transparent Film Dressing, 6x7cm (2.375" x 2.75"). Sterile. FDA UDI

Identifiers

Catalog Number
WIV-0607 FDA UDI
Primary DI / UDI-DI
00814639024623 FDA UDI
FDA Product Code
NAD FDA UDI
GMDN Term
Waterproof skin adhesive tape FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4020 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

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

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

Yes

FDA UDI

Category: Waterproof skin adhesive tape

Wound Free by Applied Dental, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Waterproof skin adhesive tape.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Applied Dental, Inc.

Sources (1)

  • FDA UDI e54aa07b-707b-4759-a793-2564f7757fe5 36 fields · synced May 31, 2026