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Schwert 23615

by A. Schweickhardt GmbH & Co. KG

Schwert 23615 is a Class I device made by A. Schweickhardt GmbH & Co. KG, listed in FDA GUDID since 21 Feb 2023 (UDI-DI E896236150), 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 NumberE896236150 UDI-DI Date21 Feb 2023ListedStatusListed 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  • Withdrawn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
Schwert
Generic name
Middle ear pick
Model / Ref / Catalog
23615
Primary DI / UDI-DI
E896236150
FDA product code
EIG
GMDN term
Middle ear pick
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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Category: Middle ear pick

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Properties

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