Schwert 4927

by A. Schweickhardt GmbH & Co. KG

Schwert 4927 is a Class I device made by A. Schweickhardt GmbH & Co. KG, listed in FDA GUDID since 23 Feb 2023 (UDI-DI E89649270), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberE89649270 UDI-DI	Date23 Feb 2023Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Schwert
Generic name: Dental prosthesis removal instrument
Model / Ref / Catalog: 4927
Description: Crown remover UNIVERSAL 15cm

Primary DI / UDI-DI: E89649270
FDA product code: EIS
GMDN term: Dental prosthesis removal instrument

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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Properties

Sterilise before use
Prescription use
Premarket exempt
Lot / batch number

Other properties (11, all answered No)