03809746

GUDID 07611819610392

KERRISON PUNCH-BAYONETED 6MM WIDTH/40 DEG ANGLE

SYNTHES (U.S.A.) LP

Spinal rongeur Spinal rongeur Spinal rongeur Spinal rongeur Spinal rongeur Spinal rongeur Spinal rongeur Spinal rongeur Spinal rongeur Spinal rongeur Spinal rongeur Spinal rongeur Spinal rongeur Spinal rongeur Spinal rongeur Spinal rongeur

• Primary Device ID: 07611819610392
• NIH Device Record Key: dd3779a2-3658-4558-a36e-a017a756838e
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 03.809.746
• Catalog Number: 03809746
• Company DUNS: 832637081
• Company Name: SYNTHES (U.S.A.) LP
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07611819610392 [Direct Marking]
GS1	10705034725819 [Primary]
HIBCC	H981038097460 [Secondary]

FDA Product Code

• LRY: PUNCH, SURGICAL

Sterilization

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

[07611819610392]

Moist Heat or Steam Sterilization

[07611819610392]

Moist Heat or Steam Sterilization

[07611819610392]

Moist Heat or Steam Sterilization

[07611819610392]

Moist Heat or Steam Sterilization

[07611819610392]

Moist Heat or Steam Sterilization

[07611819610392]

Moist Heat or Steam Sterilization

[07611819610392]

Moist Heat or Steam Sterilization

[07611819610392]

Moist Heat or Steam Sterilization

[07611819610392]

Moist Heat or Steam Sterilization

[07611819610392]

Moist Heat or Steam Sterilization

[07611819610392]

Moist Heat or Steam Sterilization

[07611819610392]

Moist Heat or Steam Sterilization

[07611819610392]

Moist Heat or Steam Sterilization

[07611819610392]

Moist Heat or Steam Sterilization

[07611819610392]

Moist Heat or Steam Sterilization

[07611819610392]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2021-10-13
• Device Publish Date: 2016-12-31

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• 10886982309112 - NA: 2021-10-25 HANDLE
• 10886982309129 - NA: 2021-10-25 4.5 LCP PROTECTION SLEEVE
• 10886982309303 - NA: 2021-10-25 12MM CANNULATED DRILL BIT
• 10886982309310 - NA: 2021-10-25 13MM CANNULATED DRILL BIT
• 10886982311498 - NA: 2021-10-25 4.2MM CALIBRATED DRILL BIT
• 10886982311580 - NA: 2021-10-25 MEASURING DEVICE