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EasyBoost Sheet ESB-RES-2029

by Seneca Devices Inc

EasyBoost Sheet ESB-RES-2029 is a Class I device made by Seneca Devices Inc, listed in FDA GUDID since 30 Sep 2026 (UDI-DI 00860004936886), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860004936886 UDI-DI Date30 Sep 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
EasyBoost Sheet
Generic name
Patient transfer/turning sheet, reusable
Model / reference
ESB-RES-2029
Primary DI / UDI-DI
00860004936886
FDA product code
FMR
GMDN term
Patient transfer/turning sheet, reusable
Device class
Class I
Regulation number
880.6785
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FMR (Device, Transfer, Patient, Manual).

Other devices from Seneca Devices Inc

See all devices from Seneca Devices Inc →

Properties

  • Premarket exempt
  • Serial number
Other properties (13, all answered No)