398758

GUDID H6793987580

REDUCTION ATTACHMENT

SYNTHES (U.S.A.) LP

Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps Surgical implant handling forceps

• Primary Device ID: H6793987580
• NIH Device Record Key: 7df82216-6ac7-4639-927f-35ac43c4f3ba
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 398.758
• Catalog Number: 398758
• Company DUNS: 832637081
• Company Name: SYNTHES (U.S.A.) LP
• Device Count: 1
• DM Exempt: true
• 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: false
• 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
• 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
• 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	10886982201614 [Primary]
HIBCC	H6793987580 [Secondary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

[H6793987580]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2021-10-13
• Device Publish Date: 2016-12-31

Devices Manufactured by SYNTHES (U.S.A.) LP

• H679022101060 - NA: 2024-02-27 2.4MM VA LOCKING SCREW STARDRIVE 6MM
• H679022221140 - NA: 2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/14MM
• H679022221160 - NA: 2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/16MM
• H679022221180 - NA: 2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/18MM
• H679022221200 - NA: 2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/20MM
• H679022221220 - NA: 2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/22MM
• H679022221240 - NA: 2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/24MM
• H679022221260 - NA: 2024-02-27 5.0MM VA LOCKING SCREW SLF-TPNG W/T25 STARDRIVE/26MM