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DermaClip

FDA UDI

Class I (US FDA UDI)

by Dermaclip Us, L.L.C.

Identity

Trade Name
DermaClip FDA UDI
Generic Name
Skin-closure adhesive strip FDA UDI
Device Name
DermaClip Large Clip, 1 Pack, 1" Closure, Standard Adhesive FDA UDI
Model / Reference
Large 1 Clip FDA UDI
Description
DermaClip Large Clip, 1 Pack, 1" Closure, Standard Adhesive FDA UDI

Identifiers

Catalog Number
61003 FDA UDI
Primary DI / UDI-DI
00853909006167 FDA UDI
FDA Product Code
KGX 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

Yes

FDA UDI

Over-the-Counter

No

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

DermaClip 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 14e97dfe-868c-46b7-86ea-efdbc02eb6ef 37 fields · synced May 30, 2026