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Disposa-Shield® A880105

by Dentsply Professional

Disposa-Shield® A880105 is a Class I device made by Dentsply Professional, listed in FDA GUDID since 23 Sep 2016 (UDI-DI D003A8801051), 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 NumberD003A8801051 UDI-DI Date23 Sep 2016ListedStatusListed 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  • Withdrawn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
Disposa-Shield®
Generic name
Cable/lead/sensor/probe cover, non-sterile
Model / reference
A880105
Primary DI / UDI-DI
D003A8801051
FDA product code
EFB, PEM
GMDN term
Cable/lead/sensor/probe cover, non-sterile
Device class
Class I
Regulation number
872.4200, 878.4370
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cable/lead/sensor/probe cover, non-sterile

Other devices from Dentsply Professional

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Properties

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