Unique Device Identification

 
Docket ID: FDA-2006-N-0172
Agency: Food and Drug Administration (FDA)
Parent Agency: Department of Health and Human Services (HHS)
Summary:
Docket Status: OPEN
Docket Details open glossary dialog  
Related RINs: None
Related Dockets: None
Short Title: Unique Device Identification
Keyword(s): improving medical device adverse event reporting, facilitating device recalls, reducing medical errors, patient safety, UDI, IDENTIFICATION, Device, Unique
Legacy ID: 2006N-0292
Type: Nonrulemaking
Center: CDRH
Docket Item Code: N
 

Primary Documents

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FDA 
Comment Period Closed
Nov 09, 2006 11:59 PM ET
Notice
Posted: 09/25/2006
ID: FDA-2006-N-0172-0006
FDA 
Comment Period Closed
Nov 09, 2006 11:59 PM ET
Notice
Posted: 08/11/2006
ID: FDA-2006-N-0172-0001
Comment Period Closed
Other
Posted: 03/19/2009
ID: FDA-2006-N-0172-0054
Comment Period Closed
Other
Posted: 03/19/2009
ID: FDA-2006-N-0172-0058
Comment Period Closed
Other
Posted: 03/19/2009
ID: FDA-2006-N-0172-0055

Supporting Documents

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Comments Not Accepted
Supporting & Related Material
Posted: 03/18/2009
ID: FDA-2006-N-0172-0020
Comments Not Accepted
Supporting & Related Material
Posted: 03/18/2009
ID: FDA-2006-N-0172-0022
Comments Not Accepted
Supporting & Related Material
Posted: 03/18/2009
ID: FDA-2006-N-0172-0025

Comments

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262
Comments Received*
*This count refers to the total comment/submissions received on this docket, as of 11:59 PM yesterday. Note: Agencies review all submissions, however some agencies may choose to redact, or withhold, certain submissions (or portions thereof) such as those containing private or proprietary information, inappropriate language, or duplicate/near duplicate examples of a mass-mail campaign. This can result in discrepancies between this count and those displayed when conducting searches on the Public Submission document type. For specific information about an agency’s public submission policy, refer to its website or the Federal Register document.