TRYPTIK Ti SPE-US 01 26-N

GUDID 07640375234827

Implant Holder Shaft with Slap Hammer

SpineArt SA

Surgical implant/trial-implant/sizer holder, reusable

• Primary Device ID: 07640375234827
• NIH Device Record Key: de90e7df-2917-4611-a08b-8c65eb7d7ac6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TRYPTIK Ti
• Version Model Number: SPE-US 01 26-N
• Catalog Number: SPE-US 01 26-N
• Company DUNS: 483016148
• Company Name: SpineArt SA
• 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: 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 Dimensions

• Length: 218 Millimeter
• Width: 12 Millimeter
• Height: 12 Millimeter
• Length: 218 Millimeter
• Width: 12 Millimeter
• Height: 12 Millimeter
• Length: 218 Millimeter
• Width: 12 Millimeter
• Height: 12 Millimeter
• Length: 218 Millimeter
• Width: 12 Millimeter
• Height: 12 Millimeter
• Length: 218 Millimeter
• Width: 12 Millimeter
• Height: 12 Millimeter
• Length: 218 Millimeter
• Width: 12 Millimeter
• Height: 12 Millimeter
• Length: 218 Millimeter
• Width: 12 Millimeter
• Height: 12 Millimeter
• Length: 218 Millimeter
• Width: 12 Millimeter
• Height: 12 Millimeter
• Length: 218 Millimeter
• Width: 12 Millimeter
• Height: 12 Millimeter
• Length: 218 Millimeter
• Width: 12 Millimeter
• Height: 12 Millimeter
• Length: 218 Millimeter
• Width: 12 Millimeter
• Height: 12 Millimeter
• Length: 218 Millimeter
• Width: 12 Millimeter
• Height: 12 Millimeter
• Length: 218 Millimeter
• Width: 12 Millimeter
• Height: 12 Millimeter
• Length: 218 Millimeter
• Width: 12 Millimeter
• Height: 12 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640375234827 [Primary]

FDA Product Code

• HWR: Driver, Prosthesis

Sterilization

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

[07640375234827]

Moist Heat or Steam Sterilization

[07640375234827]

Moist Heat or Steam Sterilization

[07640375234827]

Moist Heat or Steam Sterilization

[07640375234827]

Moist Heat or Steam Sterilization

[07640375234827]

Moist Heat or Steam Sterilization

[07640375234827]

Moist Heat or Steam Sterilization

[07640375234827]

Moist Heat or Steam Sterilization

[07640375234827]

Moist Heat or Steam Sterilization

[07640375234827]

Moist Heat or Steam Sterilization

[07640375234827]

Moist Heat or Steam Sterilization

[07640375234827]

Moist Heat or Steam Sterilization

[07640375234827]

Moist Heat or Steam Sterilization

[07640375234827]

Moist Heat or Steam Sterilization

[07640375234827]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-10-24
• Device Publish Date: 2022-10-14

On-Brand Devices [TRYPTIK Ti]

• 07640375234827: Implant Holder Shaft with Slap Hammer
• 07640375232021: ANATOMIC SMOOTH TRIAL RACK
• 07640375232014: LORDOTIC TRIAL RACK
• 07640332476499: TRYPTIK TI-LIFE HL AND XL INSTRUMENT BOX
• 07640332471050: TRYPTIK TI - EXTRA LARGE SMOOTH TRIAL RACK
• 07640332471043: TRYPTIK TI - HYPERLORDOTIC SMOOTH TRIAL RACK