62-00238

GUDID 04546540356604

DRILL GUIDE, CENTRIC, FOR 2.3MM SCREWS

Stryker Leibinger GmbH & Co. KG

Surgical drill guide, reusable

• Primary Device ID: 04546540356604
• NIH Device Record Key: f5cda898-ec93-4dce-b7d5-4732dfb8db89
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 62-00238
• Catalog Number: 62-00238
• Company DUNS: 316153956
• Company Name: Stryker Leibinger GmbH & Co. KG
• 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

Device Dimensions

• Length: 52 Millimeter
• Length: 52 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540356604 [Primary]

FDA Product Code

• HTW: BIT, DRILL

Sterilization

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

[04546540356604]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-04-06
• Device Publish Date: 2016-12-08

Devices Manufactured by Stryker Leibinger GmbH & Co. KG

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• 07613327556827 - NA: 2024-02-23 Facial iD MF 1 mesh kit