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Asp Medical PP992

by Asp Global, LLC

Asp Medical PP992 is a Class I device made by Asp Global, LLC, listed in FDA GUDID since 31 Jul 2022 (UDI-DI 00840216108509), 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 Number00840216108509 UDI-DI Date31 Jul 2022ListedStatusListed 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  • Withdrawn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
Asp Medical
Generic name
Pill crusher/splitter
Model / reference
PP992
Primary DI / UDI-DI
00840216108509
FDA product code
OHY
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

Other devices from Asp Global, LLC

See all devices from Asp Global, LLC →

Properties

  • Single use
  • Contains latex
  • Premarket exempt
Other properties (12, all answered No)