Karl Schumacher Composite Putty

GUDID 00842517102163

Regenerative Collagen Dental Bone Graft Composite

KARL SCHUMACHER DENTAL INSTRUMENT CO., INC.

Dental bone matrix implant, synthetic

• Primary Device ID: 00842517102163
• NIH Device Record Key: abf37976-faf2-4747-aed0-3c23cca61905
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Karl Schumacher Composite Putty
• Version Model Number: RCBP0200
• Company DUNS: 043957315
• Company Name: KARL SCHUMACHER DENTAL INSTRUMENT CO., 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: 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: true
• OTC Over-The-Counter: false

Device Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00842517102163 [Primary]

FDA Product Code

• LYC: Bone Grafting Material, Synthetic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-09-26

On-Brand Devices [Karl Schumacher Composite Putty]

• 00842517102316: Regenerative Collagen Dental Bone Graft Composite
• 00842517102309: Regenerative Collagen Dental Bone Graft Composite
• 00842517102163: Regenerative Collagen Dental Bone Graft Composite