LATITUDE EV™ 0030700

GUDID 00846832074686

TORNIER, INC.

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• Primary Device ID: 00846832074686
• NIH Device Record Key: 2c206743-8a72-42fa-8a45-0c89779551b2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LATITUDE EV™
• Version Model Number: 0030700
• Catalog Number: 0030700
• Company DUNS: 968990812
• Company Name: TORNIER, 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: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(888)494-7950
• Email: customerservice@tornier.com
• Phone: +1(888)494-7950
• Email: customerservice@tornier.com
• Phone: +1(888)494-7950
• Email: customerservice@tornier.com
• Phone: +1(888)494-7950
• Email: customerservice@tornier.com
• Phone: +1(888)494-7950
• Email: customerservice@tornier.com
• Phone: +1(888)494-7950
• Email: customerservice@tornier.com
• Phone: +1(888)494-7950
• Email: customerservice@tornier.com
• Phone: +1(888)494-7950
• Email: customerservice@tornier.com
• Phone: +1(888)494-7950
• Email: customerservice@tornier.com
• Phone: +1(888)494-7950
• Email: customerservice@tornier.com
• Phone: +1(888)494-7950
• Email: customerservice@tornier.com
• Phone: +1(888)494-7950
• Email: customerservice@tornier.com
• Phone: +1(888)494-7950
• Email: customerservice@tornier.com
• Phone: +1(888)494-7950
• Email: customerservice@tornier.com
• Phone: +1(888)494-7950
• Email: customerservice@tornier.com
• Phone: +1(888)494-7950
• Email: customerservice@tornier.com

Device Dimensions

• Length: 72 Millimeter
• Device Size Text, specify: 0
• Length: 72 Millimeter
• Device Size Text, specify: 0
• Length: 72 Millimeter
• Device Size Text, specify: 0
• Length: 72 Millimeter
• Device Size Text, specify: 0
• Length: 72 Millimeter
• Device Size Text, specify: 0
• Length: 72 Millimeter
• Device Size Text, specify: 0
• Length: 72 Millimeter
• Device Size Text, specify: 0
• Length: 72 Millimeter
• Device Size Text, specify: 0
• Length: 72 Millimeter
• Device Size Text, specify: 0
• Length: 72 Millimeter
• Device Size Text, specify: 0
• Length: 72 Millimeter
• Device Size Text, specify: 0
• Length: 72 Millimeter
• Device Size Text, specify: 0
• Length: 72 Millimeter
• Device Size Text, specify: 0
• Length: 72 Millimeter
• Device Size Text, specify: 0
• Length: 72 Millimeter
• Device Size Text, specify: 0
• Length: 72 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00846832074686 [Primary]

FDA Product Code

• JDC: PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-03-25
• Device Publish Date: 2020-08-12

On-Brand Devices [LATITUDE EV™]

• 00846832073986: 9030356
• 00846832073979: 9030351
• 00846832073962: 9030346
• 00846832073955: 9030341
• 00846832072965: 9030398
• 00846832072941: 9030397
• 00846832072927: 9030395
• 00846832072590: 9039005
• 00846832072576: 9039004
• 00846832072569: 9039003
• 00846832072552: 9039002
• 00846832072545: 9039001
• 00846832072538: 9039000
• 00846832072521: 0830825
• 00846832072514: 0830824
• 00846832072507: 0830823
• 00846832072491: 0830822
• 00846832072484: 0830821
• 00846832072477: 0830820
• 00846832072460: 0830819
• 00846832072453: 0830818
• 00846832072446: 0830817
• 00846832072439: 0830816
• 00846832074815: 0030721
• 00846832074808: 0030720
• 00846832074754: 0030711
• 00846832074747: 0030710
• 00846832074693: 0030701
• 00846832074686: 0030700