Angled Staple Punch

GUDID M209176550

BIOPRO, INC.

Bone awl Bone awl, reusable Bone awl, reusable Bone awl, reusable Bone awl, reusable Bone awl, reusable Bone awl, reusable

• Primary Device ID: M209176550
• NIH Device Record Key: 5209d94b-f8bd-4b87-8327-5f4c6d261738
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Angled Staple Punch
• Version Model Number: 17655
• Company DUNS: 618749857
• Company Name: BIOPRO, INC.
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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
HIBCC	M209176550 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K061798

FDA Product Code

• HWJ: Awl

Sterilization

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

[M209176550]

Moist Heat or Steam Sterilization

[M209176550]

Moist Heat or Steam Sterilization

[M209176550]

Moist Heat or Steam Sterilization

[M209176550]

Moist Heat or Steam Sterilization

[M209176550]

Moist Heat or Steam Sterilization

[M209176550]

Moist Heat or Steam Sterilization

[M209176550]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-05-09
• Device Publish Date: 2019-05-01

On-Brand Devices [Angled Staple Punch]

• M209176550: 17655
• 00810012483841: 17655