Karl Schumacher DRAPE

GUDID 00842517102217

Regenerative Collagen Dental Membrane

KARL SCHUMACHER DENTAL INSTRUMENT CO., INC.

Collagen dental regeneration membrane

• Primary Device ID: 00842517102217
• NIH Device Record Key: ed8164a3-3d44-487c-ad8e-2135e23017a5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Karl Schumacher DRAPE
• Version Model Number: RCMD2030
• 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	00842517102217 [Primary]

FDA Product Code

• NPL: Barrier, Animal Source, Intraoral

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: 2017-09-27

On-Brand Devices [Karl Schumacher DRAPE]

• 00842517102224: Regenerative Collagen Dental Membrane
• 00842517102217: Regenerative Collagen Dental Membrane
• 00842517102200: Regenerative Collagen Dental Membrane