Drapes

GUDID 04049539101839

Carl Zeiss Meditec AG

Instrument/equipment drape, single-use, sterile

• Primary Device ID: 04049539101839
• NIH Device Record Key: 22e9570b-73d6-41e4-99cb-9bb048f5b42a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Drapes
• Version Model Number: 326035-0000-000
• Company DUNS: 342228620
• Company Name: Carl Zeiss Meditec AG
• 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: true
• 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: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Dimensions

• Height: 82 Inch
• Width: 48 Inch
• Height: 209 Centimeter
• Width: 122 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04049539101839 [Primary]
GS1	04049539102102 [Package]; Package: [5 Units]; In Commercial Distribution
GS1	04049539102317 [Package]; Contains: 04049539102102; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• KKX: Drape, Surgical

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: 2016-08-22

On-Brand Devices [Drapes ]

• 04049539101839: 326035-0000-000
• 04049539101822: 326038-0000-000