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Aesculap MG742R

by Aesculap, Inc.

Aesculap MG742R is a Class I device made by Aesculap, Inc., listed in FDA GUDID since 6 May 2020 (UDI-DI 04046955086726), 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 Number04046955086726 UDI-DI Date6 May 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  • Withdrawn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
Aesculap
Generic name
Dental rongeur
Model / Ref / Catalog
MG742R
Primary DI / UDI-DI
04046955086726
FDA product code
EMG
GMDN term
Dental rongeur
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental rongeur

Similar devices

Other devices filed under FDA product code EMG (FORCEPS, TOOTH EXTRACTOR, SURGICAL).

Other devices from Aesculap, Inc.

See all devices from Aesculap, Inc. →

Properties

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