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InterDry

FDA UDI

Class I (US FDA UDI)

by Coloplast Corp.

Identity

Trade Name
InterDry FDA UDI
Generic Name
Antimicrobial skin friction/moisture control fabric, single-patient reusable FDA UDI
Device Name
InterDry. Moisture Wicking Fabric with Antimicrobial Silver. 18 in by 10 in. FDA UDI
Model / Reference
7915 FDA UDI
Description
InterDry. Moisture Wicking Fabric with Antimicrobial Silver. 18 in by 10 in. FDA UDI

Identifiers

Catalog Number
7915 FDA UDI
Primary DI / UDI-DI
00311701069730 FDA UDI
510(k) Number
K110715 FDA UDI
FDA Product Code
FRL FDA UDI
GMDN Term
Antimicrobial skin friction/moisture control fabric, single-patient reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5300 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 10 Inch FDA UDI
Length — 18 Inch FDA UDI

Category: Antimicrobial skin friction/moisture control fabric, single-patient reusable

InterDry by Coloplast Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Antimicrobial skin friction/moisture control fabric, single-patient reusable.

Cleared under the same submission

K110715 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Coloplast Corp.

Sources (1)

  • FDA UDI 1254c9c0-6798-46f8-ba69-1ef1b8c54b52 37 fields · synced May 30, 2026