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Zip PreLoc 2 Wound Closure Device PS3002

by Stryker Corp.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00853114007270 UDI-DI Date21 May 2020ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Zip PreLoc 2 Wound Closure Device
Generic Name
Adhesive bandage
Model / Ref / Catalog
PS3002
Primary DI / UDI-DI
00853114007270
FDA Product Code
MKY
GMDN Term
Adhesive bandage
Device Class
Class I
Regulation Number
878.4320
GUDID distribution status
In Commercial Distribution
Size
Width — 2 Centimeter

Related devices

Category: Adhesive bandage

Other devices from Stryker Corp.

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Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No