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N/A 4542

by Carefusion 2200, Inc GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10885403143267 UDI-DIDate23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Generic Name
Peripheral anaesthesia single-administration set, non-medicated
Model / Ref / Catalog
4542
Primary DI / UDI-DI
10885403143267
FDA Product Code
HEE
GMDN Term
Peripheral anaesthesia single-administration set, non-medicated
Device Class
Class II
Regulation Number
884.5100
GUDID distribution status
In Commercial Distribution
Size
Needle Gauge — 20 Gauge
Length — 20 Centimeter

Related devices

Category: Peripheral anaesthesia single-administration set, non-medicated

Other devices from Carefusion 2200, Inc.

See all devices from Carefusion 2200, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No