Primary Device ID | 04546540089069 |
NIH Device Record Key | 42a63f7f-c318-4cf5-a9dd-62d5c33b5c7b |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 604036 |
Catalog Number | 604036 |
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 |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Size Text, specify | 0 |
Length | 36 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04546540089069 [Primary] |
HRS | PLATE, FIXATION, BONE |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
[04546540089069]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-09-24 |
07613327606010 - REUNION | 2024-08-30 Humeral 1 Express Tray |
07613327606027 - REUNION | 2024-08-30 Humeral 1 Express Insert |
07613327606034 - REUNION | 2024-08-30 Humeral 2 Express Insert |
07613327606041 - REUNION | 2024-08-30 Reverse Express Insert |
07613327606058 - REUNION | 2024-08-30 Anatomic Express Insert |
07613327606065 - REUNION | 2024-08-30 Anatomic Express Tray |
07613327606072 - REUNION | 2024-08-30 Reverse Express Tray |
07613327606089 - REUNION | 2024-08-30 Humeral 2 Express Tray |