Symphysis Plate, 4-Hole, PRS Phoenix

GUDID 09120069818147

I.T.S. GmbH

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

• Primary Device ID: 09120069818147
• NIH Device Record Key: c4f87c81-9801-4ccd-bade-c991817cc990
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Symphysis Plate, 4-Hole, PRS Phoenix
• Version Model Number: 211621-4
• Company DUNS: 303456917
• Company Name: I.T.S. GmbH
• Device Count: 1
• DM Exempt: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	09120069818147 [Primary]

FDA Product Code

• HRS: Plate, Fixation, Bone

Sterilization

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

[09120069818147]

Moist Heat or Steam Sterilization

[09120069818147]

Moist Heat or Steam Sterilization

[09120069818147]

Moist Heat or Steam Sterilization

[09120069818147]

Moist Heat or Steam Sterilization

[09120069818147]

Moist Heat or Steam Sterilization

[09120069818147]

Moist Heat or Steam Sterilization

[09120069818147]

Moist Heat or Steam Sterilization

[09120069818147]

Moist Heat or Steam Sterilization

[09120069818147]

Moist Heat or Steam Sterilization

[09120069818147]

Moist Heat or Steam Sterilization

[09120069818147]

Moist Heat or Steam Sterilization

[09120069818147]

Moist Heat or Steam Sterilization

[09120069818147]

Moist Heat or Steam Sterilization

[09120069818147]

Moist Heat or Steam Sterilization

[09120069818147]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-10-31
• Device Publish Date: 2022-10-21

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• 09120116977896 - PF Lag Screw, L=110mm, PPS: 2024-04-11 PF Lag Screw, L=110mm, PPS
• 09120116977902 - PF Lag Screw, L=115mm, PPS: 2024-04-11 PF Lag Screw, L=115mm, PPS
• 09120116977889 - PF Lag Screw, L=105mm, PPS: 2024-04-10 PF Lag Screw, L=105mm, PPS