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1352237

by Medtronic Xomed Inc

1352237 is a Class I device made by Medtronic Xomed Inc, listed in FDA GUDID since 10 Sep 2017 (UDI-DI 00681490038263), registry data as of 8 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

Unverified

Source GUDID, synced 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00681490038263 UDI-DI Date10 Sep 2017ListedStatusListed 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  • Withdrawn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

Generic name
Tympanostomy tube inserter, reusable
Model / reference
1352237
Primary DI / UDI-DI
00681490038263
FDA product code
JYM
GMDN term
Tympanostomy tube inserter, reusable
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution

Related devices

Category: Tympanostomy tube inserter, reusable

Other devices from Medtronic Xomed Inc

See all devices from Medtronic Xomed Inc →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)