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N/A TT1615

by Carefusion 2200, Inc GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10885403090547 UDI-DIDate30 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  • Withdrawn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

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Generic Name
Soft-tissue biopsy procedure kit, non-medicated
Model / Ref / Catalog
TT1615
Primary DI / UDI-DI
10885403090547
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
Needle Gauge — 16 Gauge
Length — 15 Centimeter

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