← Back to catalogue

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 Home & Field, OTC, Standard Adhesive. 3 Packages in waterproof pouch. Each package contains 1 DermaQuik device which will close 1" of wound. FDA UDI
Model / Reference
Home & Field 3 Multi-pouch FDA UDI
Description
DermaQuik Home & Field, OTC, Standard Adhesive. 3 Packages in waterproof pouch. Each package contains 1 DermaQuik device which will close 1" of wound. FDA UDI

Identifiers

Catalog Number
62531 FDA UDI
Primary DI / UDI-DI
00853909006518 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

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

Manufacturer

Sources (1)

  • FDA UDI 1babad77-3678-4d74-8077-41176e175f1d 37 fields · synced May 30, 2026