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BaseVac 3SUR4.25-1-3P

by R. E. Morrison Equipment Inc

BaseVac 3SUR4.25-1-3P (2800080) is a Class I device made by R. E. Morrison Equipment Inc, listed in FDA GUDID since 3 Jun 2024 (UDI-DI D13028000800), 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 NumberD13028000800 UDI-DI Date3 Jun 2024ListedStatusListed 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  • Withdrawn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
BaseVac
Generic name
Dental suction system
Model / Ref / Catalog
3SUR4.25-1-3P, 2800080
Primary DI / UDI-DI
D13028000800
FDA product code
NRD
GMDN term
Dental suction system
Device class
Class I
Regulation number
872.6640
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental suction system

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Properties

  • Premarket exempt
Other properties (14, all answered No)