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Sprint 200 1ES200-521

by L I N E T spol. s r.o.

Sprint 200 1ES200-521 is a Class II device made by L I N E T spol. s r.o., listed in FDA GUDID since 2 Oct 2025 (UDI-DI 08592654542163), 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 Number08592654542163 UDI-DI Date2 Oct 2025ListedStatusListed 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  • Withdrawn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
Sprint 200
Generic name
Hospital stretcher, powered
Model / reference
1ES200-521
Primary DI / UDI-DI
08592654542163
FDA product code
INK
GMDN term
Hospital stretcher, powered
Device class
Class II
Regulation number
890.3690
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code INK (Stretcher, Wheeled, Powered).

Other devices from L I N E T spol. s r.o.

See all devices from L I N E T spol. s r.o. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)