Primary Device ID | 03596010250001 |
NIH Device Record Key | 50c50d26-4a3f-4231-8743-69d618f72f3c |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 7204775 |
Catalog Number | 7204775 |
Company DUNS | 109903521 |
Company Name | Smith & Nephew, Inc. |
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 | true |
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)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com | |
Phone | +1(800)821-5700 |
gudid@smith-nephew.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03596010250001 [Primary] |
HWC | Screw, fixation, bone |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-01-31 |
Device Publish Date | 2015-10-05 |
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