SD03501750

GUDID 10887587078274

SELF-RETAINING SCRWDRVR BLADE FOR 90°SCRWDRVR

Synthes GmbH

Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable

• Primary Device ID: 10887587078274
• NIH Device Record Key: ba4e7748-4dac-4f95-b81f-cc5814f96e2a
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: SD03.501.750
• Catalog Number: SD03501750
• Company DUNS: 486711679
• Company Name: Synthes GmbH
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10887587078274 [Primary]

FDA Product Code

• HXX: SCREWDRIVER

Sterilization

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

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

[10887587078274]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-10-20
• Device Publish Date: 2023-10-12

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• 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