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SkinPlus DP0S1-SW

by Taiwan Surgical Corporation

SkinPlus DP0S1-SW is a Class I device made by Taiwan Surgical Corporation, listed in FDA GUDID since 11 Jul 2023 (UDI-DI 04717480906031), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04717480906031 UDI-DI Date11 Jul 2023ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
SkinPlus
Generic name
Skin stapler/staple, non-bioabsorbable
Model / reference
DP0S1-SW
Primary DI / UDI-DI
04717480906031
FDA product code
QQS
GMDN term
Skin stapler/staple, non-bioabsorbable
Device class
Class I
Regulation number
878.4740
GUDID distribution status
In Commercial Distribution

Related devices

Category: Skin stapler/staple, non-bioabsorbable

Similar devices in this category

Other devices filed under Skin stapler/staple, non-bioabsorbable.

Other devices from Taiwan Surgical Corporation

See all devices from Taiwan Surgical Corporation →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)