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McKesson 108-PC1000

by Mckesson Medical-Surgical Inc.

McKesson 108-PC1000 is a Class I device made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 18 Sep 2019 (UDI-DI 00612479177246), 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 Number00612479177246 UDI-DI Date18 Sep 2019ListedStatusListed 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  • Withdrawn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
Pill crusher/splitter
Model / reference
108-PC1000
Primary DI / UDI-DI
00612479177246
FDA product code
KYW
GMDN term
Pill crusher/splitter
Device class
Class I
Regulation number
880.6430
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pill crusher/splitter

Similar devices

Other devices filed under FDA product code KYW (Container, Liquid Medication, Graduated).

Other devices from Mckesson Medical-Surgical Inc.

See all devices from Mckesson Medical-Surgical Inc. →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)