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Baltic Denture System BDLoad

by Merz Dental GmbH 1,000+ variants

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 21 Oct 2026. What this means

Regulatory status

as of registry sync 21 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD7091035456 UDI-DI Date1 Oct 2019ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic name
Preformed complete denture
Model / Ref / Catalog
Baltic Denture System BDLoad High Impact upper Sw6 PLSEbm6DFs C1 dark pink, 1035456
Primary DI / UDI-DI
D7091035456
FDA product code
EKO
GMDN term
Preformed complete denture
Device class
Class II
Regulation number
872.3600
GUDID distribution status
In Commercial Distribution

Related devices

Category: Preformed complete denture

Other devices from Merz Dental GmbH

See all devices from Merz Dental GmbH →

Properties

  • Premarket exempt
  • Lot / batch number
  • Expiration date

Other properties (12)

  • Supplied sterile: No
  • Sterilise before use: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Prescription use: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No
  • Manufacturing date: No