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TD2 Patient Kit 74011

by Nalu Medical

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00812537037127 UDI-DI Date20 Feb 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  • Withdrawn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
TD2 Patient Kit
Generic Name
Noninvasive device battery charger
Model / Reference
74011
Primary DI / UDI-DI
00812537037127
FDA Product Code
GZF, GZB
GMDN Term
Noninvasive device battery charger
Device Class
Class II
Regulation Number
882.5870, 882.5880
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Other devices from Nalu Medical

See all devices from Nalu Medical →

Properties

  • Prescription Use
  • Convenience Kit
  • Serial Number
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Expiration Date: No