Aesculap

GUDID B504GSAA804R0

Provision

Drilling power tool attachment, basic

• Primary Device ID: B504GSAA804R0
• NIH Device Record Key: 93e71878-fe4b-47aa-8e09-2bfaf33cabd5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aesculap
• Version Model Number: AA804R
• Company DUNS: 016889401
• Company Name: Provision
• Device Count: 1
• DM Exempt: true
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com
• Phone: 541-508-7520
• Email: customersupport@provisiondrs.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B504GSAA804R0 [Primary]

FDA Product Code

• KDC: Instrument, Surgical, Disposable

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-06-18
• Device Publish Date: 2024-06-10

On-Brand Devices [Aesculap]

• B504OMFF912SB0: FF912SB
• B504OMBD511R0: BD511R
• B504GSEA016R0: EA016R
• B504OMNP582R0: NP582R
• B504OMNP583R0: NP583R
• B504GSFF484R0: FF484R
• B504OMGP210SU0: GP210SU
• B504GSBC211R0: BC211R
• B504OMFF904SB0: FF904SB
• B504GSMD6050: MD605
• B504GSAA804R0: AA804R
• B504OMOL322R0: OL322R
• B504OMOL321R0: OL321R
• B504OMFL666R0: FL666R