Primary Device ID | 00889024039056 |
NIH Device Record Key | cedb54d4-8927-48e0-8db8-4dec01a542e4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pressure Sentinel® |
Version Model Number | 2228-22 |
Catalog Number | 00-2228-022-00 |
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 |
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 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 Issuing Agency | Device ID |
---|---|
GS1 | 00889024039056 [Primary] |
HWE | INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00889024039056]
Moist Heat or Steam Sterilization
[00889024039056]
Moist Heat or Steam Sterilization
[00889024039056]
Moist Heat or Steam Sterilization
[00889024039056]
Moist Heat or Steam Sterilization
[00889024039056]
Moist Heat or Steam Sterilization
[00889024039056]
Moist Heat or Steam Sterilization
[00889024039056]
Moist Heat or Steam Sterilization
[00889024039056]
Moist Heat or Steam Sterilization
[00889024039056]
Moist Heat or Steam Sterilization
[00889024039056]
Moist Heat or Steam Sterilization
[00889024039056]
Moist Heat or Steam Sterilization
[00889024039056]
Moist Heat or Steam Sterilization
[00889024039056]
Moist Heat or Steam Sterilization
[00889024039056]
Moist Heat or Steam Sterilization
[00889024039056]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-08-12 |
Device Publish Date | 2016-07-26 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() PRESSURE SENTINEL 75009347 2100060 Live/Registered |
ZIMMER, INC. 1995-10-23 |