Primary Device ID | 07613327349771 |
NIH Device Record Key | ab088620-45b4-4f5c-a194-6df81ee96126 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | T2 |
Version Model Number | 2380-0808S |
Catalog Number | 2380-0808S |
Company DUNS | 481999654 |
Company Name | Stryker Trauma SA |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Size Text, specify | 0 |
Length | 80 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327349771 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-21 |
Device Publish Date | 2020-07-13 |
07613327349870 | Nail with Compression Screw |
07613327349863 | End Cap |
07613327349856 | Nail with Compression Screw |
07613327349849 | Nail with Compression Screw |
07613327349832 | End Cap |
07613327349825 | End Cap |
07613327349818 | Nail with Compression Screw |
07613327349801 | Nail with Compression Screw |
07613327349795 | Nail with Compression Screw |
07613327349788 | Nail with Compression Screw |
07613327349771 | Nail with Compression Screw |
07613327349764 | End Cap |
07613327349757 | End Cap |
07613327349740 | Nail with Compression Screw |
07613327349733 | Nail with Compression Screw |
07613327349726 | End Cap |
07613327349719 | Nail with Compression Screw |
07613327349702 | End Cap |
07613327349696 | Nail with Compression Screw |
07613327349689 | End Cap |
07613327349672 | End Cap |
07613327349665 | End Cap |
07613327349658 | Nail with Compression Screw |
07613327349641 | Nail with Compression Screw |
07613327349634 | End Cap |
07613327349627 | Nail with Compression Screw |
07613327349610 | Nail with Compression Screw |
07613327349603 | End Cap |
07613327349597 | End Cap |
07613327349580 | Nail with Compression Screw |
07613327349573 | Nail with Compression Screw |
07613327349566 | Nail with Compression Screw |
07613327349559 | Nail with Compression Screw |
07613327349542 | Nail with Compression Screw |
04546540654939 | Target Device Recon |
07613327510171 | 2351-0335S |
07613327503876 | 2339-0922S |
07613327503869 | 2339-1222S |
07613327503852 | 2339-1422S |
07613327503845 | 2339-1022S |
07613327503838 | 2339-1122S |
07613327503821 | 2339-1322S |
07613327479782 | Femur Retrograde Indication Tray |
07613327479775 | Femur Retrograde Insert |
07613327479768 | Femur Retrograde Proximal Targeting Tray |
07613327423976 | 2351-0330 |
07613327423969 | 2351-0335 |
07613327411843 | 2353-3907 |
07613327411805 | 2353-3906 |
07613327411782 | 2353-3908 |