Distraction Screws Caspar type 800-501x

GUDID 00810607000279

Distraction Screws Caspar type Quantity 10 DI 810607000262

ACRA-CUT INC

Intraoperative bone pin/screw, sterile Intraoperative bone pin/screw, sterile Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use

• Primary Device ID: 00810607000279
• NIH Device Record Key: c2b9926f-33c9-424d-aa41-d68aa6b95eba
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Distraction Screws Caspar type
• Version Model Number: 800-501x
• Catalog Number: 800-501x
• Company DUNS: 612611459
• Company Name: ACRA-CUT INC
• 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: 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 9782632210
• Email: info@acracut.com
• Phone: 9782632210
• Email: info@acracut.com
• Phone: 9782632210
• Email: info@acracut.com
• Phone: 9782632210
• Email: info@acracut.com
• Phone: 9782632210
• Email: info@acracut.com
• Phone: 9782632210
• Email: info@acracut.com
• Phone: 9782632210
• Email: info@acracut.com
• Phone: 9782632210
• Email: info@acracut.com
• Phone: 9782632210
• Email: info@acracut.com
• Phone: 9782632210
• Email: info@acracut.com
• Phone: 9782632210
• Email: info@acracut.com
• Phone: 9782632210
• Email: info@acracut.com
• Phone: 9782632210
• Email: info@acracut.com
• Phone: 9782632210
• Email: info@acracut.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810607000279 [Primary]

FDA Product Code

• KDC: Instrument, Surgical, Disposable

Sterilization

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

[00810607000279]

Radiation Sterilization

[00810607000279]

Radiation Sterilization

[00810607000279]

Radiation Sterilization

[00810607000279]

Radiation Sterilization

[00810607000279]

Radiation Sterilization

[00810607000279]

Radiation Sterilization

[00810607000279]

Radiation Sterilization

[00810607000279]

Radiation Sterilization

[00810607000279]

Radiation Sterilization

[00810607000279]

Radiation Sterilization

[00810607000279]

Radiation Sterilization

[00810607000279]

Radiation Sterilization

[00810607000279]

Radiation Sterilization

[00810607000279]

Radiation Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-05-01

On-Brand Devices [Distraction Screws Caspar type]

• 00810607000293: Distraction Screws Caspar type Quantity 10 DI 810607000286
• 00810607000286: Distraction Screws Caspar type
• 00810607000279: Distraction Screws Caspar type Quantity 10 DI 810607000262
• 00810607000262: Distraction Screws Caspar type
• 00810607000255: Distraction Screws Caspar type Quantity 10 DI 810607000248
• 00810607000231: Distraction Screws Caspar type Quantity 10 DI 810607000224
• 00810607000224: Distraction Screws Caspar type