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Superslide 31608

by Therafin Corporation

Superslide 31608 is a Class I device made by Therafin Corporation, listed in FDA GUDID since 6 Jul 2023 (UDI-DI 00840252910241), 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 Number00840252910241 UDI-DI Date6 Jul 2023ListedStatusListed 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  • Withdrawn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
Superslide
Generic name
Patient transfer sliding board
Model / Ref / Catalog
31608
Primary DI / UDI-DI
00840252910241
FDA product code
IKX
GMDN term
Patient transfer sliding board
Device class
Class I
Regulation number
890.5050
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code IKX (Aid, Transfer).

Other devices from Therafin Corporation

See all devices from Therafin Corporation →

Properties

  • Premarket exempt
  • Manufacturing date
Other properties (13, all answered No)