03164030

GUDID 07612334216830

TEMPORARY FIXATION WIRE Ø2.5MM LENGTH 150MM

Synthes GmbH

Orthopaedic bone wire Orthopaedic guidewire, single-use Orthopaedic guidewire, single-use Orthopaedic guidewire, single-use Orthopaedic guidewire, single-use Orthopaedic guidewire, single-use Orthopaedic guidewire, single-use Orthopaedic guidewire, single-use Orthopaedic guidewire, single-use Orthopaedic guidewire, single-use Orthopaedic guidewire, single-use Orthopaedic guidewire, single-use Orthopaedic guidewire, single-use Orthopaedic guidewire, single-use

• Primary Device ID: 07612334216830
• NIH Device Record Key: 59465bb3-b629-4d4b-b1af-72734c027059
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 03.164.030
• Catalog Number: 03164030
• Company DUNS: 486711679
• Company Name: Synthes GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	07612334216830 [Direct Marking]
GS1	10886982311238 [Primary]

FDA Product Code

• LXH: Orthopedic manual surgical instrument

Sterilization

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

[07612334216830]

Moist Heat or Steam Sterilization

[07612334216830]

Moist Heat or Steam Sterilization

[07612334216830]

Moist Heat or Steam Sterilization

[07612334216830]

Moist Heat or Steam Sterilization

[07612334216830]

Moist Heat or Steam Sterilization

[07612334216830]

Moist Heat or Steam Sterilization

[07612334216830]

Moist Heat or Steam Sterilization

[07612334216830]

Moist Heat or Steam Sterilization

[07612334216830]

Moist Heat or Steam Sterilization

[07612334216830]

Moist Heat or Steam Sterilization

[07612334216830]

Moist Heat or Steam Sterilization

[07612334216830]

Moist Heat or Steam Sterilization

[07612334216830]

Moist Heat or Steam Sterilization

[07612334216830]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-12-07
• Device Publish Date: 2022-11-29

Devices Manufactured by Synthes GmbH

• 10887587078366 - NA: 2024-05-22 BONE PUSHER
• 10886982344229 - NA: 2024-05-13 FOOT - 10MM UPRIGHT REDUCTION CLAMP
• 10886982344236 - NA: 2024-05-13 FOOT - 4MM UPRIGHT REDUCTION CLAMP
• 10886982344243 - NA: 2024-05-13 HOOK - 4MM UPRIGHT REDUCTION CLAMP
• 10886982344250 - NA: 2024-05-13 HOOK - 10MM UPRIGHT REDUCTION CLAMP
• 10886982346940 - NA: 2024-05-09 60MM DEPTH PROBE FOR XL25 SCREWS
• 10886982346933 - NA: 2024-05-08 EXTENDED MULTI HOLE WIRE GUIDE FOR RFNA
• 10886982346957 - NA: 2024-05-08 FNS ANGLED GUIDE 130° W/ WIDER BASE