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Flexi-Needle 7016

by Liberty Medical Inc 24 variants

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 NumberB16570160328083126144 UDI-DI Date18 Aug 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Flexi-Needle
Generic Name
General-purpose brachytherapy system applicator, manual
Model / Reference
7016
Primary DI / UDI-DI
B16570160328083126144
FDA Product Code
IWJ
GMDN Term
General-purpose brachytherapy system applicator, manual
Device Class
Class I
Regulation Number
892.5650
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

Other devices from Liberty Medical Inc

See all devices from Liberty Medical Inc →

Properties

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

Other properties (8)

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