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EF1 904-07-0000

by Medshape, Inc.

EF1 904-07-0000 is a Class I device made by Medshape, Inc., listed in FDA GUDID since 31 Mar 2026 (UDI-DI 00190446959809), 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 Number00190446959809 UDI-DI Date31 Mar 2026ListedStatusListed 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  • Withdrawn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
EF1
Generic name
Surgical torque wrench, reusable
Model / reference
904-07-0000
Primary DI / UDI-DI
00190446959809
FDA product code
HXC
GMDN term
Surgical torque wrench, reusable
Device class
Class I
Regulation number
888.4540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code HXC (WRENCH).

Other devices from Medshape, Inc.

See all devices from Medshape, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)