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5888-00-60

by Zimmer, 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

Source GUDID, synced 10 Nov 2026.

Regulatory status

as of registry sync 10 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00889024200463 UDI-DI Date22 Dec 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  • Withdrawn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
Device sterilization/disinfection container, reusable
Model / Ref / Catalog
5888-00-60, 00-5888-000-60
Primary DI / UDI-DI
00889024200463
FDA product code
FSM
GMDN term
Device sterilization/disinfection container, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Depth — 152.4 Millimeter

Overview

AI-generated summary, 10 Nov 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

5888-00-60 is a surgical instrument tray. This device is a reusable sterilization or disinfection container that measures 152.4 Millimeter in depth. It must be sterilized before use via moist heat or steam sterilization.

This device is classified as Class I. It is identified by product code FSM under regulation number 878.4800. The device is currently in commercial distribution.

Similar devices in this category

Other devices filed under Device sterilization/disinfection container, reusable.

Other devices from Zimmer, Inc.

See all devices from Zimmer, Inc. →

Questions

AI-generated answers, 10 Nov 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the 5888-00-60?

    It is recorded under the GMDN device type "Device sterilization/disinfection container, reusable", which GMDN defines as "A receptacle designed to hold wrapped and/or unwrapped medical/dental devices in a chemical washer/disinfector and/or sterilizer during the washing/disinfection and/or sterilization cycle(s)". FDA lists it under the product name "Tray, Surgical, Instrument". It is recorded as Class I.

  • What are the product code and regulation of the 5888-00-60?

    FDA records the 5888-00-60 under product code FSM and regulation number 878.4800.

  • Who makes the 5888-00-60?

    Zimmer, Inc. is the manufacturer on record for the 5888-00-60.

Properties

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