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Aspiration Handpiece L-1331

by A1 Medical GmbH GUDID

Listed (no authorization) FDA GUDID database listing only

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04251047930003 UDI-DIDate29 May 2026ListedStatusIn distribution

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
Aspiration Handpiece
Generic Name
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable
Model / Reference
L-1331
Primary DI / UDI-DI
04251047930003
FDA Product Code
KYG
GMDN Term
Ophthalmic irrigation/infusion/aspiration cannula, non-illuminating, reusable
Device Class
Class I
Regulation Number
886.4360
Commercial Distribution
In Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Other devices from A1 Medical GmbH

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Properties

  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (11)

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