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Surgical Direct SD91143005

by Surgical Direct, Inc.

Surgical Direct SD91143005 is a Class I device made by Surgical Direct, Inc., listed in FDA GUDID since 30 Nov 2022 (UDI-DI B382SD911430050), 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 NumberB382SD911430050 UDI-DI Date30 Nov 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  • Withdrawn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
Surgical Direct
Generic name
Suction system catheter, general-purpose
Model / Ref / Catalog
SD91143005
Primary DI / UDI-DI
B382SD911430050
FDA product code
KCB
GMDN term
Suction system catheter, general-purpose
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Suction system catheter, general-purpose

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)