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Monoart Bib Up!

by Euronda SpA 12 variants

Monoart Bib Up! (22030004) is a Class I device made by Euronda SpA, listed in FDA GUDID since 10 Apr 2025 (UDI-DI E307220300040), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberE307220300040 UDI-DI Date10 Apr 2025ListedStatusListed 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  • Withdrawn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
Monoart
Generic name
Patient examination/treatment drape, single-use
Model / Ref / Catalog
Monoart Bib Up!, 22030004
Primary DI / UDI-DI
E307220300040
FDA product code
KHR
GMDN term
Patient examination/treatment drape, single-use
Device class
Class I
Regulation number
872.6050
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KHR (Absorber, Saliva, Paper).

Other devices from Euronda SpA

See all devices from Euronda SpA →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)