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SkinPlus

FDA UDI

Class I (US FDA UDI)

by Taiwan Surgical Corporation

Identity

Trade Name
SkinPlus FDA UDI
Generic Name
Skin stapler/staple, non-bioabsorbable FDA UDI
Device Name
Disposable Skin Stapler, Wide, 35 staples FDA UDI
Model / Reference
DP0S1-SW FDA UDI
Description
Disposable Skin Stapler, Wide, 35 staples FDA UDI

Identifiers

Primary DI / UDI-DI
04717480906031 FDA UDI
FDA Product Code
QQS FDA UDI
GMDN Term
Skin stapler/staple, non-bioabsorbable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4740 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

Yes

FDA UDI

Category: Skin stapler/staple, non-bioabsorbable

SkinPlus by Taiwan Surgical Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Skin stapler/staple, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 3e607e42-e515-4ee3-be94-fae44ce0acfb 33 fields · synced Jun 1, 2026