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Pivot Rail 10469

by Dynarex Corp.

Pivot Rail 10469 is a bedrail (FDA Class II; FDA product code FNL, Bed, Ac-Powered Adjustable Hospital) made by Dynarex Corp., listed in FDA GUDID since 7 Mar 2019 (UDI-DI 00616784046914), 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 Number00616784046914 UDI-DI Date7 Mar 2019ListedStatusListed 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  • Withdrawn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
Pivot Rail
Generic name
Bedrail
Model / reference
10469
Primary DI / UDI-DI
00616784046914
FDA product code
FNL
GMDN term
Bedrail
Device class
Class II
Regulation number
880.5100
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Similar devices

Other devices filed under FDA product code FNL (Bed, Ac-Powered Adjustable Hospital).

Other devices from Dynarex Corp.

See all devices from Dynarex Corp. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)