DSM PV012SU

GUDID 04046955207114

STERILE DRAPE

Aesculap AG

Medical equipment drape, single-use Medical equipment drape, single-use

• Primary Device ID: 04046955207114
• NIH Device Record Key: aebc7512-fa08-410c-8e2c-5bd1f2407468
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DSM
• Version Model Number: PV012SU
• Catalog Number: PV012SU
• Company DUNS: 315018218
• Company Name: Aesculap AG
• Device Count: 5
• 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: 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

Customer Support Contacts

• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com
• Phone: +1(800)282-9000
• Email: GUDID.BBMUS_Service@bbraun.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04046955207114 [Unit of Use]
GS1	04046955207121 [Primary]

FDA Product Code

• PUI: Drape, surgical, exempt

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-07-01
• Device Publish Date: 2020-05-04

On-Brand Devices [DSM]

• 04046955207114: STERILE DRAPE
• 04046955206766: FOOT SWITCH WIRELESS