Continuum®
GUDID 00889024154582
Zimmer, Inc.
Acetabulum prosthesis trial, reusable| Primary Device ID | 00889024154582 |
| NIH Device Record Key | 5e8b482d-13d8-4391-9688-1de729c5ac0a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Continuum® |
| Version Model Number | 00-8835-022-32 |
| Company DUNS | 056038268 |
| Company Name | Zimmer, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
| Device Size Text, specify | 0 |
| Lumen/Inner Diameter | 32 Millimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024154582 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K103662
FDA Product Code
| LZO | Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
[00889024154582]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2016-08-31 |
On-Brand Devices [Continuum®]
| 00889024154889 | 00-8838-023-36 |
| 00889024154872 | 00-8838-023-32 |
| 00889024154865 | 00-8838-022-36 |
| 00889024154858 | 00-8838-022-32 |
| 00889024154612 | 00-8835-023-36 |
| 00889024154605 | 00-8835-023-32 |
| 00889024154599 | 00-8835-022-36 |
| 00889024154582 | 00-8835-022-32 |
| 00889024154292 | 00-8834-023-36 |
| 00889024154285 | 00-8834-022-36 |
| 00889024153998 | 00-8832-023-36 |
| 00889024153981 | 00-8832-023-32 |
| 00889024153974 | 00-8832-022-36 |
| 00889024153967 | 00-8832-022-32 |
| 00889024153523 | 00-8831-023-40 |
| 00889024153516 | 00-8831-023-36 |
| 00889024153509 | 00-8831-022-40 |
| 00889024153493 | 00-8831-022-36 |
| 00889024151192 | 00-8757-000-02 |
| 00889024151185 | 00-8757-000-01 |
Trademark Results [Continuum]
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