Skip to content

CHI2320

by Bard Peripheral Vascular

CHI2320 is a Class I device made by Bard Peripheral Vascular, listed in FDA GUDID since 18 Jul 2018 (UDI-DI 10885403088988), 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 Number10885403088988 UDI-DI Date18 Jul 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  • Withdrawn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

Generic name
Cell-block cytology aspiration needle
Model / Ref / Catalog
CHI2320
Primary DI / UDI-DI
10885403088988
FDA product code
GAA
GMDN term
Cell-block cytology aspiration needle
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Size
Length — 20 Centimeter

Related devices

Category: Cell-block cytology aspiration needle

Similar devices

Other devices filed under FDA product code GAA (NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE).

Other devices from Bard Peripheral Vascular

See all devices from Bard Peripheral Vascular →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)