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Midwest 6-Pin Coupler, K-Style CE 2.004.0422

by SycoTec GmbH & Co. KG

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberESAN68905241 UDI-DI Date6 Aug 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  • Withdrawn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

Trade Name
Midwest 6-Pin Coupler, K-Style CE
Generic Name
Pneumatic dental handpiece coupler
Model / Ref / Catalog
2.004.0422, 6890524
Primary DI / UDI-DI
ESAN68905241
FDA Product Code
EFB
GMDN Term
Pneumatic dental handpiece coupler
Device Class
Class I
Regulation Number
872.4200
GUDID distribution status
In Commercial Distribution

Properties

  • Prescription Use
  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No