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N/A TT1415

by Carefusion 2200, Inc

Listed FDA GUDID listing, not in commercial distribution

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10885403090516 UDI-DI Date30 Sep 2016ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Generic Name
Soft-tissue biopsy procedure kit, non-medicated
Model / Ref / Catalog
TT1415
Primary DI / UDI-DI
10885403090516
FDA Product Code
FCG
GMDN Term
Soft-tissue biopsy procedure kit, non-medicated
Device Class
Class II
Regulation Number
876.1075
GUDID distribution status
Not in Commercial Distribution
Size
Length — 15 Centimeter
Needle Gauge — 14 Gauge

Other devices from Carefusion 2200, Inc.

See all devices from Carefusion 2200, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No