Skip to content

Bevel T34E

by Medtronic Sofamor Danek, Inc.

Bevel T34E is a Class I device made by Medtronic Sofamor Danek, Inc., listed in FDA GUDID since 6 Nov 2020 (UDI-DI 00763000311759), 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 Number00763000311759 UDI-DI Date6 Nov 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  • Withdrawn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
Bevel
Generic name
Bone access channel kit
Model / reference
T34E
Primary DI / UDI-DI
00763000311759
FDA product code
LXH
GMDN term
Bone access channel kit
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code LXH (ORTHOPEDIC MANUAL SURGICAL INSTRUMENT).

Other devices from Medtronic Sofamor Danek, Inc.

See all devices from Medtronic Sofamor Danek, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)