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Aesculap MD551R

by Aesculap, Inc.

Aesculap MD551R is a Class I device made by Aesculap, Inc., listed in FDA GUDID since 24 Sep 2016 (UDI-DI 04046964570490), 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 Number04046964570490 UDI-DI Date24 Sep 2016ListedStatusListed 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  • Withdrawn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
Surgical/emergency suction cannula, non-illuminating, reusable
Model / Ref / Catalog
MD551R
Primary DI / UDI-DI
04046964570490
FDA product code
GEA
GMDN term
Surgical/emergency suction cannula, non-illuminating, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical/emergency suction cannula, non-illuminating, reusable

Similar devices in this category

Other devices filed under Surgical/emergency suction cannula, non-illuminating, reusable.

Other devices from Aesculap, Inc.

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Properties

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