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Truform® 1926BL-M

by Surgical Appliance Industries, Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00048503513511 UDI-DI Date17 Dec 2025ListedStatusListed 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  • Withdrawn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
Truform®
Generic name
Compression/pressure sock/stocking, single-use
Model / reference
1926BL-M
Primary DI / UDI-DI
00048503513511
FDA product code
DWL
GMDN term
Compression/pressure sock/stocking, single-use
Device class
Class II
Regulation number
880.5780
GUDID distribution status
In Commercial Distribution

Other devices from Surgical Appliance Industries, Inc.

See all devices from Surgical Appliance Industries, Inc. →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number

Other properties (12)

  • Supplied sterile: No
  • Sterilise before use: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Prescription use: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No