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AHIP Internal Trigger Point Wand 1112

by New Pelvic Pain Technologies

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 Number00862945000404 UDI-DI Date29 Nov 2023ListedStatusListed 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  • Withdrawn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
AHIP Internal Trigger Point Wand
Generic Name
Pelvic floor internal manual massager
Model / Reference
1112
Primary DI / UDI-DI
00862945000404
FDA Product Code
OSD
GMDN Term
Pelvic floor internal manual massager
Device Class
Class II
Regulation Number
890.5670
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pelvic floor internal manual massager

Similar devices

Also classified as Pelvic floor internal manual massager.

Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

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