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Scancoat 102-Scb

by Domico Med-Device, LLC

Scancoat 102-Scb is a Class I device made by Domico Med-Device, LLC, listed in FDA GUDID since 24 Sep 2020 (UDI-DI 00810050241892), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810050241892 UDI-DI Date24 Sep 2020ListedStatusListed 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  • Withdrawn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
Scancoat
Generic name
Multifunction body cushion
Model / reference
102-SCB
Primary DI / UDI-DI
00810050241892
FDA product code
IWY, CCX
GMDN term
Multifunction body cushion
Device class
Class I
Regulation number
892.1920, 868.6820
GUDID distribution status
In Commercial Distribution

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Category: Multifunction body cushionRadiological headrest

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Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)