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Wexler Surgical, Inc. SHA-RB6

by Wexler Surgical, 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 NumberM944SHARB60 UDI-DI Date10 Oct 2025ListedStatusListed 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  • Withdrawn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
Wexler Surgical, Inc.
Generic Name
Diamond ENT bur, single-use
Model / Reference
SHA-RB6
Primary DI / UDI-DI
M944SHARB60
FDA Product Code
EQJ
GMDN Term
Diamond ENT bur, single-use
Device Class
Class I
Regulation Number
874.4140
GUDID distribution status
In Commercial Distribution

Other devices from Wexler Surgical, Inc.

See all devices from Wexler Surgical, Inc. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No