Aesculap GN090

Aesculap GN090 is a Class II device made by Aesculap AG, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04038653078103), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04038653078103 UDI-DI	Date23 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 04038653078103

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Aesculap
Generic name: Surgical irrigation/aspiration pump, reusable
Model / Ref / Catalog: GN090

Primary DI / UDI-DI: 04038653078103
FDA product code: GEI
GMDN term: Surgical irrigation/aspiration pump, reusable

Device class: Class II
Regulation number: 878.4400
GUDID distribution status: In Commercial Distribution

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Properties

Prescription use
Serial number

Other properties (13, all answered No)