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Rusch IPN044981

by Teleflex Incorporated

Rusch IPN044981 (556000-000000) is a general-body orifice lubricant (FDA Class I; FDA product code KMJ, Lubricant, patient) made by Teleflex Incorporated, listed in FDA GUDID since 15 Sep 2018 (UDI-DI 24026704067620), 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 Number24026704067620 UDI-DI Date15 Sep 2018ListedStatusListed 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  • Withdrawn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
Rusch
Generic name
General-body orifice lubricant, non-sterile
Model / Ref / Catalog
IPN044981, 556000-000000
Primary DI / UDI-DI
24026704067620
FDA product code
KMJ
GMDN term
General-body orifice lubricant, non-sterile
Device class
Class I
Regulation number
880.6375
GUDID distribution status
In Commercial Distribution
Size
Total Volume — 500 Milliliter

Similar devices

Other devices filed under FDA product code KMJ (Lubricant, patient).

Other devices from Teleflex Incorporated

  • Arrow IPNB00820 Open recall

    Class II
  • Arrow IPNB00826 Open recall

    Class II
  • Arrow IPNB00822 Open recall

    Class II
  • Arrow IPNB00827 Open recall

    Class II

See all devices from Teleflex Incorporated →

Properties

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