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Elan 4 MD798

by Aesculap, Inc.

Elan 4 MD798 is a Class I device made by Aesculap, Inc., listed in FDA GUDID since 27 Oct 2020 (UDI-DI 04046955138975), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04046955138975 UDI-DI Date27 Oct 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  • Withdrawn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
Elan 4
Generic name
Burring power tool attachment
Model / Ref / Catalog
MD798
Primary DI / UDI-DI
04046955138975
FDA product code
GEY
GMDN term
Burring power tool attachment
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Burring power tool attachment

Similar devices in this category

Other devices filed under Burring power tool attachment.

Other devices from Aesculap, Inc.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)