Skip to content

ULCL500

by Zimmer Orthopaedic Surgical Products

ULCL500 (UL-CL500) is a Class I device made by Zimmer Orthopaedic Surgical Products, listed in FDA GUDID since 27 Sep 2016 (UDI-DI 00889024471177), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00889024471177 UDI-DI Date27 Sep 2016ListedStatusListed 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  • Withdrawn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

Generic name
Surgical fluid/smoke waste management system suction unit
Model / Ref / Catalog
ULCL500, UL-CL500
Primary DI / UDI-DI
00889024471177
FDA product code
GCY
GMDN term
Surgical fluid/smoke waste management system suction unit
Device class
Class I
Regulation number
878.4680
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code GCY (APPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED).

Other devices from Zimmer Orthopaedic Surgical Products

See all devices from Zimmer Orthopaedic Surgical Products →

Properties

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