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Merocel® 400152

by Medtronic Xomed Inc

Merocel 400152 is an ear wick (FDA Class I; FDA product code KCN, Ear Wick) made by Medtronic Xomed Inc, listed in FDA GUDID since 9 Sep 2017 (UDI-DI 20681490104580), 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 Number20681490104580 UDI-DI Date9 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  • Withdrawn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

Trade name
Merocel®
Generic name
Ear wick, non-biodegradable
Model / reference
400152
Primary DI / UDI-DI
20681490104580
FDA product code
KCN
GMDN term
Ear wick, non-biodegradable
Device class
Class I
Regulation number
874.5220
GUDID distribution status
In Commercial Distribution
Size
Outer Diameter — 5.0 Millimeter

Related devices

Category: Ear wick, non-biodegradable

Similar devices in this category

Other devices filed under Ear wick, non-biodegradable.

Other devices from Medtronic Xomed Inc

See all devices from Medtronic Xomed Inc →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (10, all answered No)