OPMI® Drapes

GUDID 04049539101310

Carl Zeiss Meditec AG

Instrument/equipment drape, single-use, sterile

• Primary Device ID: 04049539101310
• NIH Device Record Key: bd6dfa54-5d40-4f31-b05e-58212afc47da
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OPMI® Drapes
• Version Model Number: 326084-0000-000
• 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: 13 Inch
• Width: 14.25 Inch
• Height: 33 Centimeter
• Width: 36 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04049539101310 [Primary]
GS1	04049539102126 [Package]; Package: [10 Units]; In Commercial Distribution
GS1	04049539102331 [Package]; Contains: 04049539102126; Package: [6 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 [OPMI® Drapes ]

• 04049539101310: 326084-0000-000
• 04049539102171: 326044-0000-000