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Dynamic Tissue Systems™

FDA UDI

Class I (US FDA UDI)

by Southmedic Incorporated

Identity

Trade Name
Dynamic Tissue Systems™ FDA UDI
Generic Name
Skin-closing tension device FDA UDI
Device Name
Cannulator FDA UDI
Model / Reference
SWC01 FDA UDI
Description
Cannulator FDA UDI

Identifiers

Catalog Number
SWC01 FDA UDI
Primary DI / UDI-DI
10620974002335 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Skin-closing tension device FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Category: Skin-closing tension device

Dynamic Tissue Systems™ by Southmedic Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin-closing tension device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Southmedic Incorporated

Sources (1)

  • FDA UDI 03253a5e-a060-4775-8cf2-07509975aa21 35 fields · synced May 31, 2026