Pressure Sentinel® 00-2228-097-00
GUDID 00889024039209
Zimmer, Inc.
Orthopaedic prosthesis implantation instrument, reusable| Primary Device ID | 00889024039209 |
| NIH Device Record Key | c5aef8df-7905-4d44-a653-4c2e0ddcb375 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pressure Sentinel® |
| Version Model Number | 2228-97 |
| Catalog Number | 00-2228-097-00 |
| 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
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com | |
| Phone | +1(800)348-2759 |
| zimmer.consumerrelations@zimmerbiomet.com |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00889024039209 [Primary] |
FDA Product Code
| LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00889024039209]
Moist Heat or Steam Sterilization
[00889024039209]
Moist Heat or Steam Sterilization
[00889024039209]
Moist Heat or Steam Sterilization
[00889024039209]
Moist Heat or Steam Sterilization
[00889024039209]
Moist Heat or Steam Sterilization
[00889024039209]
Moist Heat or Steam Sterilization
[00889024039209]
Moist Heat or Steam Sterilization
[00889024039209]
Moist Heat or Steam Sterilization
[00889024039209]
Moist Heat or Steam Sterilization
[00889024039209]
Moist Heat or Steam Sterilization
[00889024039209]
Moist Heat or Steam Sterilization
[00889024039209]
Moist Heat or Steam Sterilization
[00889024039209]
Moist Heat or Steam Sterilization
[00889024039209]
Moist Heat or Steam Sterilization
[00889024039209]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-08-12 |
| Device Publish Date | 2017-01-31 |
On-Brand Devices [Pressure Sentinel®]
Trademark Results [Pressure Sentinel]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PRESSURE SENTINEL 75009347 2100060 Live/Registered |
ZIMMER, INC. 1995-10-23 |
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