pezo-P™ PEEK cage family CS 3302-08

GUDID 04052536015191

pezo-P, height 8 mm, length 29 mm, angle 5°

Ulrich GmbH & Co. KG

Polymeric spinal fusion cage, sterile

• Primary Device ID: 04052536015191
• NIH Device Record Key: 0d5a8851-e610-493c-8d48-7fc66b5e9117
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: pezo-P™ PEEK cage family
• Version Model Number: CS 3302-08
• Catalog Number: CS 3302-08
• Company DUNS: 315494757
• Company Name: Ulrich GmbH & Co. KG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: 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: +4907319654152
• Email: safety@ulrichmedical.com
• Phone: +4907319654152
• Email: safety@ulrichmedical.com
• Phone: +4907319654152
• Email: safety@ulrichmedical.com
• Phone: +4907319654152
• Email: safety@ulrichmedical.com
• Phone: +4907319654152
• Email: safety@ulrichmedical.com
• Phone: +4907319654152
• Email: safety@ulrichmedical.com
• Phone: +4907319654152
• Email: safety@ulrichmedical.com
• Phone: +4907319654152
• Email: safety@ulrichmedical.com
• Phone: +4907319654152
• Email: safety@ulrichmedical.com
• Phone: +4907319654152
• Email: safety@ulrichmedical.com
• Phone: +4907319654152
• Email: safety@ulrichmedical.com
• Phone: +4907319654152
• Email: safety@ulrichmedical.com
• Phone: +4907319654152
• Email: safety@ulrichmedical.com
• Phone: +4907319654152
• Email: safety@ulrichmedical.com
• Phone: +4907319654152
• Email: safety@ulrichmedical.com
• Phone: +4907319654152
• Email: safety@ulrichmedical.com
• Phone: +4907319654152
• Email: safety@ulrichmedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04052536015191 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K103814

FDA Product Code

• MAX: Intervertebral fusion device with bone graft, lumbar

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-07-30

On-Brand Devices [pezo-P™ PEEK cage family]

• 04052536015450: pezo-P, height 14 mm, length 29 mm, angle 12°
• 04052536015436: pezo-P, height 13 mm, length 29 mm, angle 12°
• 04052536015412: pezo-P, height 12 mm, length 29 mm, angle 12°
• 04052536015399: pezo-P, height 11 mm, length 29 mm, angle 12°
• 04052536015375: pezo-P, height 10 mm, length 29 mm, angle 12°
• 04052536015351: pezo-P, height 9 mm, length 29 mm, angle 12°
• 04052536015337: pezo-P, height 8 mm, length 29 mm, angle 12°
• 04052536015313: pezo-P, height 14 mm, length 29 mm, angle 5°
• 04052536015290: pezo-P, height 13 mm, length 29 mm, angle 5°
• 04052536015276: pezo-P, height 12 mm, length 29 mm, angle 5°
• 04052536015252: pezo-P, height 11 mm, length 29 mm, angle 5°
• 04052536015238: pezo-P, height 10 mm, length 29 mm, angle 5°
• 04052536015214: pezo-P, height 9 mm, length 29 mm, angle 5°
• 04052536015191: pezo-P, height 8 mm, length 29 mm, angle 5°
• 04052536015177: pezo-P, height 7 mm, length 29 mm, angle 5°
• 04052536015153: pezo-P, height 14 mm, length 24 mm, angle 5°
• 04052536015139: pezo-P, height 13 mm, length 24 mm, angle 5°
• 04052536015115: pezo-P, height 12 mm, length 24 mm, angle 5°
• 04052536015092: pezo-P, height 11 mm, length 24 mm, angle 5°
• 04052536015078: pezo-P, height 10 mm, length 24 mm, angle 5°
• 04052536015054: pezo-P, height 9 mm, length 24 mm, angle 5°
• 04052536015030: pezo-P, height 8 mm, length 24 mm, angle 5°
• 04052536015016: pezo-P, height 7 mm, length 24 mm, angle 5°