DEVICE: 3M™ SmartClip™ Dimpled Nitinol Super-Elastic OrthoForm™ (00652221114976)
Device Identifier (DI) Information
3M™ SmartClip™ Dimpled Nitinol Super-Elastic OrthoForm™
9296-913
In Commercial Distribution
9296-913
3M UNITEK CORPORATION
9296-913
In Commercial Distribution
9296-913
3M UNITEK CORPORATION
9296-913 SmartClip™ Dimpled Nitinol Super-Elastic OrthoForm™ III Ovoid U .016 U/Use 10/Pk
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
No | |
Yes | |
Yes | |
No | |
No | |
No | |
No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
41397 | Orthodontic archwire |
A dental wire in the shape of an arch used with orthodontic attachments (orthodontic brackets) that are affixed to the crowns/surfaces of two or more teeth in order to cause/guide tooth movement. This is a single-patient device intended to be used for the duration of the treatment (single-use) before being discarded.
|
Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
DZC | WIRE, ORTHODONTIC |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
---|
No storage/handling found |
Clinically Relevant Size
[?]Size Type Text |
---|
No Device Sizes |
Device Record Status
c49a27e8-27a1-43fd-863b-4e3933631180
December 16, 2022
1
December 08, 2022
December 16, 2022
1
December 08, 2022
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
No Package DIs found |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
---|---|
No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
80652221114972
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+1(800)228-3957
3Mhealthcarecompliance@mmm.com
3Mhealthcarecompliance@mmm.com