03164000

GUDID 07612334216533

SIZING TRIAL F/ 3.5MM INTRAPEL ACET PL LARGE RIGHT STANDARD

Synthes GmbH

Surgical implant template, reusable

• Primary Device ID: 07612334216533
• NIH Device Record Key: eb4cb6bc-6eb0-4c8b-a632-29fd415860e9
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 03.164.000
• Catalog Number: 03164000
• Company DUNS: 486711679
• Company Name: Synthes GmbH
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07612334216533 [Direct Marking]
GS1	10886982310996 [Primary]

FDA Product Code

• HWT: TEMPLATE

Sterilization

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

[07612334216533]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-12-07
• Device Publish Date: 2022-11-29

Devices Manufactured by Synthes GmbH

• 10886982350435 - NA: 2026-02-19 HALF BENNETT SMALL/LEFT
• 10886982350442 - NA: 2026-02-19 HALF BENNETT SMALL/RIGHT
• 10886982350459 - NA: 2026-02-19 HALF BENNETT LARGE/LEFT
• 10886982350466 - NA: 2026-02-19 HALF BENNETT LARGE/RIGHT
• 10886982351579 - NA: 2026-02-19 SHOULDER HOOK 2.2 MM TIP / 235 MM LENGTH
• 10886982351661 - NA: 2026-02-19 T-HANDLE AO CONNECTOR
• 10886982351678 - NA: 2026-02-19 T-HANDLE LARGE AO CONNECTOR
• 10886982361288 - NA: 2026-02-19 5MM AWL, QC