Rasp Up Bend 20° 901131st

GUDID 10810190015855

T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION

Bone file/rasp, manual, reusable

• Primary Device ID: 10810190015855
• NIH Device Record Key: b6b9526e-9f37-4385-9239-28eb28feadd6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rasp Up Bend 20°
• Version Model Number: F
• Catalog Number: 901131st
• Company DUNS: 534123013
• Company Name: T.A.G MEDICAL PRODUCTS AGRICULTURAL COOPERATIVE ASSOCIATION
• 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: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10810190015855 [Primary]

FDA Product Code

• HTP: File

Sterilization

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

[10810190015855]

Moist Heat or Steam Sterilization

[10810190015855]

Moist Heat or Steam Sterilization

[10810190015855]

Moist Heat or Steam Sterilization

[10810190015855]

Moist Heat or Steam Sterilization

[10810190015855]

Moist Heat or Steam Sterilization

[10810190015855]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2022-06-10
• Device Publish Date: 2016-09-24

On-Brand Devices [Rasp Up Bend 20°]

• 10810190018160: B
• 10810190015855: F
• 10810190014933: B
• 10810190014063: B
• 10818674026625: 901131p