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InHealth Technologies PK 2002F-R2

by Freudenberg Medical LLC

Listed FDA GUDID listing, not in commercial distribution

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 Number00848253001401 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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
InHealth Technologies
Generic Name
Laryngectomy tube
Model / Reference
PK 2002F-R2
Primary DI / UDI-DI
00848253001401
FDA Product Code
BYD, BTR, BTO, JOH
GMDN Term
Laryngectomy tube
Device Class
Class I
Regulation Number
868.5375, 868.5730, 868.5800
GUDID distribution status
Not in Commercial Distribution

Other devices from Freudenberg Medical LLC

See all devices from Freudenberg Medical LLC →

Properties

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

Other properties (9)

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