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hi-slip® full plus HS.FPM4020

by Oasis Medikal Urunler Kimya Turizm Sanayi Ve Ticaret Anonim Sirketi

Listed FDA GUDID listing, not in commercial distribution

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number08697749683544 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
hi-slip® full plus
Generic Name
Single-administration urethral catheterization kit, single-use
Model / Ref / Catalog
HS.FPM4020
Primary DI / UDI-DI
08697749683544
FDA Product Code
EZD
GMDN Term
Single-administration urethral catheterization kit, single-use
Device Class
Class II
Regulation Number
876.5130
GUDID distribution status
Not in Commercial Distribution
Size
Length — 16 Inch
Catheter Gauge — 20 French

Properties

  • Sterile
  • Single Use
  • Convenience Kit
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No