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HoverSling Repositioning Sheet HMSLING-50RSS-HC

by Hovertech International

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 Number00816299013276 UDI-DI Date12 May 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  • Withdrawn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
HoverSling Repositioning Sheet
Generic Name
General-purpose patient lifting system sling/harness
Model / Reference
HMSLING-50RSS-HC
Primary DI / UDI-DI
00816299013276
FDA Product Code
FRZ
GMDN Term
General-purpose patient lifting system sling/harness
Device Class
Class II
Regulation Number
880.6775
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Conditional

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Properties

  • Convenience Kit
  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (10)

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