T2 2351-0330

GUDID 07613327423976

Stryker Trauma SA

Surgical screwdriver, reusable

• Primary Device ID: 07613327423976
• NIH Device Record Key: 0505b30d-5a1c-436b-8c86-15415d086993
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: T2
• Version Model Number: 2351-0330
• Catalog Number: 2351-0330
• Company DUNS: 481999654
• Company Name: Stryker Trauma SA
• 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: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327423976 [Primary]

FDA Product Code

• HXX: SCREWDRIVER

Sterilization

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

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

[07613327423976]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-07-02
• Device Publish Date: 2021-06-24

On-Brand Devices [T2]

• 07613327349870: Nail with Compression Screw
• 07613327349863: End Cap
• 07613327349856: Nail with Compression Screw
• 07613327349849: Nail with Compression Screw
• 07613327349832: End Cap
• 07613327349825: End Cap
• 07613327349818: Nail with Compression Screw
• 07613327349801: Nail with Compression Screw
• 07613327349795: Nail with Compression Screw
• 07613327349788: Nail with Compression Screw
• 07613327349771: Nail with Compression Screw
• 07613327349764: End Cap
• 07613327349757: End Cap
• 07613327349740: Nail with Compression Screw
• 07613327349733: Nail with Compression Screw
• 07613327349726: End Cap
• 07613327349719: Nail with Compression Screw
• 07613327349702: End Cap
• 07613327349696: Nail with Compression Screw
• 07613327349689: End Cap
• 07613327349672: End Cap
• 07613327349665: End Cap
• 07613327349658: Nail with Compression Screw
• 07613327349641: Nail with Compression Screw
• 07613327349634: End Cap
• 07613327349627: Nail with Compression Screw
• 07613327349610: Nail with Compression Screw
• 07613327349603: End Cap
• 07613327349597: End Cap
• 07613327349580: Nail with Compression Screw
• 07613327349573: Nail with Compression Screw
• 07613327349566: Nail with Compression Screw
• 07613327349559: Nail with Compression Screw
• 07613327349542: Nail with Compression Screw
• 04546540654939: Target Device Recon
• 07613327510171: 2351-0335S
• 07613327503876: 2339-0922S
• 07613327503869: 2339-1222S
• 07613327503852: 2339-1422S
• 07613327503845: 2339-1022S
• 07613327503838: 2339-1122S
• 07613327503821: 2339-1322S
• 07613327479782: Femur Retrograde Indication Tray
• 07613327479775: Femur Retrograde Insert
• 07613327479768: Femur Retrograde Proximal Targeting Tray
• 07613327423976: 2351-0330
• 07613327423969: 2351-0335
• 07613327411843: 2353-3907
• 07613327411805: 2353-3906
• 07613327411782: 2353-3908