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McKesson 16-LC02-REFILL

by Mckesson Medical-Surgical Inc.

McKesson 16-LC02-REFILL is an ENT illuminating foreign body extraction set (FDA Class I; FDA product code JYG, Curette, Ear) made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 9 Sep 2024 (UDI-DI 00612479269569), 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 Number00612479269569 UDI-DI Date9 Sep 2024ListedStatusListed 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  • Withdrawn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
McKesson
Generic name
ENT illuminating foreign body extraction set
Model / reference
16-LC02-REFILL
Primary DI / UDI-DI
00612479269569
FDA product code
JYG
GMDN term
ENT illuminating foreign body extraction set
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution

Related devices

Category: ENT illuminating foreign body extraction set

Similar devices

Other devices filed under FDA product code JYG (Curette, Ear).

Other devices from Mckesson Medical-Surgical Inc.

See all devices from Mckesson Medical-Surgical Inc. →

Properties

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