Ambi/Classic XT001031-2

GUDID 00885556654309

INTRMED PLT 110 DEG 3H W/ 4MM OFFSET

Smith & Nephew, Inc.

Orthopaedic fixation plate, non-bioabsorbable, sterile
Primary Device ID00885556654309
NIH Device Record Key2ae53144-42ca-44f7-926b-d051ced9197e
Commercial Distribution StatusIn Commercial Distribution
Brand NameAmbi/Classic
Version Model NumberXT001031-2
Catalog NumberXT001031-2
Company DUNS109903521
Company NameSmith & Nephew, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM
Phone+1(800)238-7538
EmailGUDID@SMITH-NEPHEW.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS100885556654309 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KTTAPPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


[00885556654309]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-06-24

On-Brand Devices [Ambi/Classic]

00885556654309INTRMED PLT 110 DEG 3H W/ 4MM OFFSET
00885556654293INTRMED PLT 100 DEG 3H W/ 4MM OFFSET

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.