← Back to catalogue

Dynamic Tissue Systems™

FDA UDI

Class II (US FDA UDI)

by Southmedic Incorporated

Identity

Trade Name
Dynamic Tissue Systems™ FDA UDI
Generic Name
Skin-closure adhesive strip FDA UDI
Device Name
ABRA® Adhesive Skin Closure Set FDA UDI
Model / Reference
CWM02A FDA UDI
Description
ABRA® Adhesive Skin Closure Set FDA UDI

Identifiers

Catalog Number
CWM02A FDA UDI
Primary DI / UDI-DI
10620974001802 FDA UDI
FDA Product Code
LRO FDA UDI
GMDN Term
Skin-closure adhesive strip FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4370 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

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

Yes

FDA UDI

Category: Skin-closure adhesive strip

Dynamic Tissue Systems™ by Southmedic Incorporated — Class II — 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 0b42f56b-eaa6-4985-9216-56a45533e5c5 36 fields · synced May 29, 2026