Procedure Chair

GUDID 00817463026641

3 Section Top; 27" Width; 120V Electric 817463026641 PCEXG327197425TTZZF6

OAKWORKS, INC.

Examination/treatment table, line-powered

• Primary Device ID: 00817463026641
• NIH Device Record Key: 2243cc6d-92bf-4c92-9c48-1a3000702f65
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Procedure Chair
• Version Model Number: 100 Procedure Chair / PCG Chair
• Company DUNS: 130256837
• Company Name: OAKWORKS, INC.
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817463026641 [Primary]

FDA Product Code

• LGX: Table, Examination, Medical, Powered

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-08-28
• Device Publish Date: 2023-08-19

On-Brand Devices [Procedure Chair]

• 00817463027020: 3 Section Top; 26" Width; 120V Electric PCG3X6T310USXXXX
• 00817463026641: 3 Section Top; 27" Width; 120V Electric 817463026641 PCEXG327197425TTZZF6
• 00817463027037: 3050 Procedure Chair 3 Section Top; 26" Width; 120V Electric 817463027037 PCG3X6T310US2ACS
• 00817463027044: 3100 Procedure Chair 3 Section Top; 26" Width; 120V Electric 817463027044 PCG3X6T311USRECS