Skip to content

Supracor Stimulite Honeycomb SMRT1615

by Supracor, Inc. GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00842749101859 UDI-DIDate4 Oct 2022ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name
Supracor Stimulite Honeycomb
Generic Name
Wheelchair seat cushion
Model / Reference
SMRT1615
Primary DI / UDI-DI
00842749101859
FDA Product Code
IMP
GMDN Term
Wheelchair seat cushion
Device Class
Class I
Regulation Number
890.3920
GUDID distribution status
Not in Commercial Distribution

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No