CORB® 00-3240-063-00
GUDID 00889024066304
Zimmer, Inc.
Sterilization/disinfection container| Primary Device ID | 00889024066304 |
| NIH Device Record Key | ca3c106e-86b6-4a2a-9dac-009d9361fd4f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CORB® |
| Version Model Number | 3240-63 |
| Catalog Number | 00-3240-063-00 |
| Company DUNS | 056038268 |
| Company Name | Zimmer, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Dimensions
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024066304 [Primary] |
FDA Product Code
| FSM | TRAY, SURGICAL, INSTRUMENT |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
[00889024066304]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-10-08 |
| Device Publish Date | 2017-05-09 |
On-Brand Devices [CORB®]
| 00889024066328 | 3240-65 |
| 00889024066311 | 3240-64 |
| 00889024066304 | 3240-63 |
| 00889024066298 | 3240-62 |
| 00889024066267 | 3240-43 |
| 00889024066250 | 3240-42 |
| 00889024066243 | 3240-41 |
| 00889024066236 | 3240-33 |
| 00889024066229 | 3240-32 |
| 00889024066212 | 3240-31 |
| 00889024066205 | 3240-23 |
| 00889024066199 | 3240-22 |
| 00889024066182 | 3240-21 |
| 00889024066175 | 3240-13 |
| 00889024066168 | 3240-12 |
| 00889024066151 | 3240-11 |
| 00889024066144 | 3240-01 |
Trademark Results [CORB]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 CORB 74246396 1730887 Live/Registered |
ZIMMER, INC 1992-02-14 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.