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Span-America SPAN AIDS

by Span-America Medical Systems, Inc. 146 variants

Span-America SPAN AIDS (SP418-000) is a Class I device made by Span-America Medical Systems, Inc., listed in FDA GUDID since 7 Dec 2022 (UDI-DI H933SP418000), 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 NumberH933SP418000 UDI-DI Date7 Dec 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Span-America
Generic name
Freestanding patient positioner, single-use
Model / Ref / Catalog
SPAN AIDS, SP418-000
Description
GEO LAM POS RPLCMT STRIP 6ST/C (P01408)
Primary DI / UDI-DI
H933SP418000
FDA product code
KIC
GMDN term
Freestanding patient positioner, single-use
Device class
Class I
Regulation number
890.3175
GUDID distribution status
In Commercial Distribution

Related devices

Category: Freestanding patient positioner, single-use

Other devices from Span-America Medical Systems, Inc.

See all devices from Span-America Medical Systems, Inc. →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)