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INUMI Flex Needle GTI-00054

by Galvanize Therapeutics, Inc. United States GUDID

Product code OAB

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850031859173 UDI-DIDate14 May 2026ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — GUDID listing Listed

Recalls: none on record (FDA, checked 22 Oct 2026)

Specification

GUDID · synced 22 Oct 2026

Trade Name
INUMI Flex Needle
Generic Name
Irreversible electroporation system endoscopic probe
Model / Reference
GTI-00054
Primary DI / UDI-DI
00850031859173
510(k) Number
FDA Product Code
OAB, GEI
GMDN Term
Irreversible electroporation system endoscopic probe
Device Class
Class II
Regulation Number
878.4400
Commercial Distribution
In Commercial Distribution
MRI Safety
MR Unsafe

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Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Single Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date
Other properties (9)
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No

Sources (1)

  • FDA UDI 970e75b6-3d3c-4377-a5bb-41475886648b 34 fields · synced 22 Oct 2026