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N/A BAT3015

by Carefusion 2200, Inc

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

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 Number10885403056949 UDI-DI Date21 Sep 2017ListedStatusListed GUDID: 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  • Withdrawn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
Bone marrow biopsy procedure kit
Model / Ref / Catalog
BAT3015
Primary DI / UDI-DI
10885403056949
FDA Product Code
LWE, FMI
GMDN Term
Bone marrow biopsy procedure kit
Device Class
Class II
Regulation Number
880.5570
GUDID distribution status
In Commercial Distribution
Size
Needle Gauge — 15 Gauge
Length — 3 Inch

Related devices

Category: Bone marrow biopsy procedure kit

Other devices from Carefusion 2200, Inc.

See all devices from Carefusion 2200, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Convenience Kit
  • Combination Product
  • Lot / Batch Number
  • Expiration Date

Other properties (7)

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