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Surgical Direct SD90321945SC

by Surgical Direct, Inc.

Surgical Direct SD90321945SC is a Class I device made by Surgical Direct, Inc., listed in FDA GUDID since 14 Jun 2023 (UDI-DI B382SD90321945SC0), 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 NumberB382SD90321945SC0 UDI-DI Date14 Jun 2023ListedStatusListed 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  • Withdrawn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
Surgical Direct
Generic name
General-purpose surgical scissors, single-use
Model / Ref / Catalog
SD90321945SC
Primary DI / UDI-DI
B382SD90321945SC0
FDA product code
EGN
GMDN term
General-purpose surgical scissors, single-use
Device class
Class I
Regulation number
872.4565
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: General-purpose surgical scissors, single-use

Similar devices

Other devices filed under FDA product code EGN (Scissors, Surgical Tissue, Dental).

Other devices from Surgical Direct, Inc.

See all devices from Surgical Direct, Inc. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)