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Zetuvit Plus

by Paul Hartmann Corp. 2 variants

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 Number04052199777429 UDI-DI Date20 Jan 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial
Model / Ref / Catalog
413602 Zetuvit Plus Shapes Multisite P10 C6, 413602
Primary DI / UDI-DI
04052199777429
FDA Product Code
NAC
GMDN Term
Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial
Device Class
Class I
Regulation Number
878.4018
GUDID distribution status
In Commercial Distribution

Other devices from Paul Hartmann Corp.

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Properties

  • Sterile
  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No