Primary Device ID | 00889024012530 |
NIH Device Record Key | 6a564de6-4d14-4d54-86b9-54c779cc176d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Spline Implant System |
Version Model Number | 1734 |
Company DUNS | 103167086 |
Company Name | ZIMMER DENTAL INC. |
Device Count | 1 |
DM Exempt | true |
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 | true |
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)854-7019 |
zimmer.consumerrelations@zimmer.com | |
Phone | +1(800)854-7019 |
zimmer.consumerrelations@zimmer.com | |
Phone | +1(800)854-7019 |
zimmer.consumerrelations@zimmer.com | |
Phone | +1(800)854-7019 |
zimmer.consumerrelations@zimmer.com | |
Phone | +1(800)854-7019 |
zimmer.consumerrelations@zimmer.com | |
Phone | +1(800)854-7019 |
zimmer.consumerrelations@zimmer.com | |
Phone | +1(800)854-7019 |
zimmer.consumerrelations@zimmer.com | |
Phone | +1(800)854-7019 |
zimmer.consumerrelations@zimmer.com | |
Phone | +1(800)854-7019 |
zimmer.consumerrelations@zimmer.com | |
Phone | +1(800)854-7019 |
zimmer.consumerrelations@zimmer.com | |
Phone | +1(800)854-7019 |
zimmer.consumerrelations@zimmer.com | |
Phone | +1(800)854-7019 |
zimmer.consumerrelations@zimmer.com | |
Phone | +1(800)854-7019 |
zimmer.consumerrelations@zimmer.com | |
Phone | +1(800)854-7019 |
zimmer.consumerrelations@zimmer.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 Issuing Agency | Device ID |
---|---|
GS1 | 00889024012530 [Primary] |
DZE | IMPLANT, ENDOSSEOUS, ROOT-FORM |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00889024012530]
Moist Heat or Steam Sterilization
[00889024012530]
Moist Heat or Steam Sterilization
[00889024012530]
Moist Heat or Steam Sterilization
[00889024012530]
Moist Heat or Steam Sterilization
[00889024012530]
Moist Heat or Steam Sterilization
[00889024012530]
Moist Heat or Steam Sterilization
[00889024012530]
Moist Heat or Steam Sterilization
[00889024012530]
Moist Heat or Steam Sterilization
[00889024012530]
Moist Heat or Steam Sterilization
[00889024012530]
Moist Heat or Steam Sterilization
[00889024012530]
Moist Heat or Steam Sterilization
[00889024012530]
Moist Heat or Steam Sterilization
[00889024012530]
Moist Heat or Steam Sterilization
[00889024012530]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2015-10-23 |
00889024013353 | 2178 |
00889024013346 | 2177 |
00889024013322 | 2174 |
00889024012820 | 1833 |
00889024012752 | 1826 |
00889024012554 | 1736 |
00889024012547 | 1735 |
00889024012530 | 1734 |
00889024012523 | 1733 |
00889024012516 | 1732 |
00889024012509 | 1731 |
00889024012240 | 1643 |
00889024012233 | 1642 |
00889024012226 | 1641 |
00889024012219 | 1640 |
00889024012202 | 1639 |
00889024012196 | 1638 |
00889024012189 | 1637 |
00889024012172 | 1636 |
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00889024012103 | 1612 |
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00889024011991 | 1576 |
00889024011984 | 1575 |
00889024011977 | 1574 |
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00889024011687 | 1500 |