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Butterfly Wound Closures

FDA UDI

Class I (US FDA UDI)

by Dynarex Corp.

Identity

Trade Name
Butterfly Wound Closures FDA UDI
Generic Name
Butterfly skin-closure adhesive strip FDA UDI
Device Name
Butterfly Wound Closures Sterile with Non-stick Pad, Medium, 3/8"x1 13/16" FDA UDI
Model / Reference
3615 FDA UDI
Description
Butterfly Wound Closures Sterile with Non-stick Pad, Medium, 3/8"x1 13/16" FDA UDI

Identifiers

Primary DI / UDI-DI
00616784361529 FDA UDI
FDA Product Code
KGX FDA UDI
GMDN Term
Butterfly 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Butterfly skin-closure adhesive strip

Butterfly Wound Closures by Dynarex Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Butterfly skin-closure adhesive strip.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dynarex Corp.

Sources (1)

  • FDA UDI a19d6015-d3ea-4763-b685-84b9a26d3a0b 33 fields · synced May 30, 2026