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WESTCOTT Scissors 09.102.11

by Dimeda Instrumente GmbH GUDID

Listed FDA GUDID listing, not in commercial distribution

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04042796016595 UDI-DIDate15 May 2017ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
WESTCOTT Scissors
Generic Name
Intraocular scissors, conventional-hinge, reusable
Model / Reference
09.102.11
Primary DI / UDI-DI
04042796016595
FDA Product Code
HNF
GMDN Term
Intraocular scissors, conventional-hinge, reusable
Device Class
Class I
Regulation Number
886.4350
GUDID distribution status
Not in Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization
Size
Length — 11 Centimeter

Other devices from Dimeda Instrumente GmbH

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No