Padgett Replacement Dermatome Blades Non-Sterile 9.1999NS

GUDID 98500107790293

Padgett Replacement Dermatome Blades Non-Sterile 100mm

Robbins Instruments Inc

Dermatome blade, single-use

• Primary Device ID: 98500107790293
• NIH Device Record Key: be57faba-b5ec-49ec-be80-c84c280011b0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Padgett Replacement Dermatome Blades Non-Sterile
• Version Model Number: 9.1999NS
• Catalog Number: 9.1999NS
• Company DUNS: 002182269
• Company Name: Robbins Instruments Inc
• Device Count: 10
• 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: false
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(973)635-8972
• Email: info@robbinsinstruments.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	18500107790297 [Unit of Use]
GS1	98500107790293 [Primary]

FDA Product Code

• GFA: BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL

Sterilization

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

[98500107790293]

Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-11-04
• Device Publish Date: 2019-10-25

On-Brand Devices [Padgett Replacement Dermatome Blades Non-Sterile]

• 98500107790293: Padgett Replacement Dermatome Blades Non-Sterile 100mm
• 90850010779297: Padgett Replacement Dermatome Blades Non-Sterile 100mm