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devemed 2429-30

by devemed GmbH

devemed 2429-30 is a Class I device made by devemed GmbH, listed in FDA GUDID since 6 Apr 2020 (UDI-DI 04061644032846), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04061644032846 UDI-DI Date6 Apr 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
devemed
Generic name
Dental suction system cannula, reusable
Model / reference
2429-30
Description
dev-aspir 1 | Suction cannula tip Ø4.0mm Insert for # 2429-00 | with slot front: Ø 6.0/5.0mm; back: Ø 6.0/5.0mm
Primary DI / UDI-DI
04061644032846
FDA product code
KCB
GMDN term
Dental suction system cannula, reusable
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental suction system cannula, reusable

Other devices from devemed GmbH

See all devices from devemed GmbH →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)