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DermaQuik

FDA UDI

Class I (US FDA UDI)

by Dermaclip Us, L.L.C.

Identity

Trade Name
DermaQuik FDA UDI
Generic Name
Skin-closure adhesive strip FDA UDI
Device Name
DermaQuik Sport & Extreme, OTC, Enhanced Adhesive. 3 Packages in waterproof pouch. Each package contains 1 DermaQuik device which will close 1" of wound. FDA UDI
Model / Reference
Sport & Extreme 3 Multi-pouch FDA UDI
Description
DermaQuik Sport & Extreme, OTC, Enhanced Adhesive. 3 Packages in waterproof pouch. Each package contains 1 DermaQuik device which will close 1" of wound. FDA UDI

Identifiers

Catalog Number
62532 FDA UDI
Primary DI / UDI-DI
00853909006525 FDA UDI
FDA Product Code
PYO FDA UDI
GMDN Term
Skin-closure adhesive strip FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5240 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

No

FDA UDI

Dimensions & Sizes

Size
Width — 21 Millimeter FDA UDI

Category: Skin-closure adhesive strip

DermaQuik by Dermaclip Us, L.L.C. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin-closure adhesive strip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 10fe3933-f8f6-4b2b-b583-e7a824ac8da0 37 fields · synced May 31, 2026