DTGQ2

GUDID 03700569625030

NEWCLIP TECHNICS

Orthopaedic fixation plate, non-bioabsorbable, non-sterile

• Primary Device ID: 03700569625030
• NIH Device Record Key: 6a6642fd-e764-4b0b-a0e9-c4b586425e2a
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: DTGQ2
• Catalog Number: DTGQ2
• Company DUNS: 263281904
• Company Name: NEWCLIP TECHNICS
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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	03700569625030 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170843

FDA Product Code

• HRS: Plate, Fixation, Bone

Sterilization

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

[03700569625030]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2024-02-19
• Device Publish Date: 2017-07-26

Devices Manufactured by NEWCLIP TECHNICS

• 03700569600839 - NA: 2024-02-19
• 03700569600846 - NA: 2024-02-19
• 03700569600853 - NA: 2024-02-19
• 03700569600860 - NA: 2024-02-19
• 03700569600877 - NA: 2024-02-19
• 03700569600884 - NA: 2024-02-19
• 03700569601027 - NA: 2024-02-19
• 03700569601188 - NA: 2024-02-19