Identity
- Trade Name
- DermaQuik FDA UDI
- Generic Name
- Skin-closure adhesive strip FDA UDI
- Device Name
- DermaQuik Sport & Extreme Wound Closure Kit, OTC. Waterproof kit includes 2 Packages of DermaQuik Sport & Extreme Devices (1 Clip per Package, 1" Closure per Package), Enhanced Adhesive. Kit also includes 2 gauze pads, 2 alcohol swabs, 2 wound dressings. All products are packaged individually within the kit and are sterile. FDA UDI
- Model / Reference
- Sport & Extreme Wound Closure Kit FDA UDI
- Description
- DermaQuik Sport & Extreme Wound Closure Kit, OTC. Waterproof kit includes 2 Packages of DermaQuik Sport & Extreme Devices (1 Clip per Package, 1" Closure per Package), Enhanced Adhesive. Kit also includes 2 gauze pads, 2 alcohol swabs, 2 wound dressings. All products are packaged individually within the kit and are sterile. FDA UDI
Identifiers
- Catalog Number
- 62552 FDA UDI
- Primary DI / UDI-DI
- 00853909006365 FDA UDI
- GMDN Term
- Skin-closure adhesive strip FDA UDI
Classification
- 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
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
Dimensions & Sizes
- Size
- Width — 21 Millimeter FDA UDI
Category: Skin-closure adhesive strip
DermaQuik by Dermaclip Us, L.L.C. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Skin-closure adhesive strip.
- UC Strip™ — Derma Sciences Canada, Inc · Class I
- 3M™ Steri-Strip™ — 3M COMPANY · Class I
- Suture Strip® — Derma Sciences Canada, Inc · Class I
- 3M™ Steri-Strip™ — 3M COMPANY · Class I
- BContak — BRIDON, CORP. · Class III
- 3M™ Steri-Strip™ — 3M COMPANY · Class I
- CareOne — Ahold U.S.A., Inc. · Class I
- DeRoyal — DEROYAL INDUSTRIES, INC. · Class I
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | N/A | Pending data |
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Manufacturer
- Manufacturer
- Dermaclip Us, L.L.C.
Sources (1)
- FDA UDI be2b4945-9109-4185-a0ad-934ebe0864b1 37 fields · synced May 30, 2026