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Aesculap FT650T

by Aesculap, Inc.

Aesculap FT650T is a Class II device made by Aesculap, Inc., listed in FDA GUDID since 24 Sep 2015 (UDI-DI 04038653171231), 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

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04038653171231 UDI-DI Date24 Sep 2015ListedStatusListed 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  • Withdrawn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
Aneurysm clip
Model / Ref / Catalog
FT650T
Primary DI / UDI-DI
04038653171231
FDA product code
HCH
GMDN term
Aneurysm clip
Device class
Class II
Regulation number
882.5200
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

Related devices

Category: Aneurysm clip

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Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Serial number
  • Expiration date
Other properties (9, all answered No)