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HoverSling Repositioning Sheet HMSLING-39RS-HC

by Hovertech International GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00816299013191 UDI-DIDate12 May 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
HoverSling Repositioning Sheet
Generic Name
General-purpose patient lifting system sling/harness
Model / Reference
HMSLING-39RS-HC
Primary DI / UDI-DI
00816299013191
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