Skip to content

Arrow IPNB00825

by Teleflex Incorporated

Arrow IPNB00825 (FB-19609-K) is a Class II device made by Teleflex Incorporated, listed in FDA GUDID since 26 Oct 2026 (UDI-DI 10801902228250), registry data as of 9 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10801902228250 UDI-DI Date26 Oct 2026ListedStatusListed 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  • Withdrawn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
Arrow
Generic name
Peripheral anaesthesia catheter set, non-medicated
Model / Ref / Catalog
IPNB00825, FB-19609-K
Primary DI / UDI-DI
10801902228250
FDA product code
CAZ
GMDN term
Peripheral anaesthesia catheter set, non-medicated
Device class
Class II
Regulation number
868.5140
GUDID distribution status
In Commercial Distribution
MRI safety
MR Conditional

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

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)