Primary Device ID | 00886385019093 |
NIH Device Record Key | 4c5a20ff-cfc9-4219-827a-070310dfe145 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 933-0027 |
Catalog Number | 933-0027 |
Company DUNS | 481999654 |
Company Name | Stryker Trauma SA |
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 | 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 |
Length | 15 Millimeter |
Length | 15 Millimeter |
Length | 15 Millimeter |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Size Text, specify | 0 |
Length | 15 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00886385019093 [Primary] |
NTG | Prosthesis, ankle, uncemented, non-constrained |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
[00886385019093]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2015-09-24 |
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