Skip to content

seca 405

by seca GmbH & Co. KG

seca 405 (4050000009) is a Class I device made by seca GmbH & Co. KG, listed in FDA GUDID since 1 May 2024 (UDI-DI 04012030021630), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04012030021630 UDI-DI Date1 May 2024ListedStatusListed 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  • Withdrawn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

Generic name
Fixed ramp
Model / Ref / Catalog
405, 4050000009
Primary DI / UDI-DI
04012030021630
FDA product code
FRW
GMDN term
Fixed ramp
Device class
Class I
Regulation number
880.2720
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FRW (SCALE, PATIENT).

Other devices from seca GmbH & Co. KG

See all devices from seca GmbH & Co. KG →

Properties

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