UltraLast™

GUDID 10816843020474

REUSABLE ULTRALAST CUP ELECTRODES: 9 MM MOLDED GOLD DISC, 4 FT. (1.2 M), SINGLE, KEVLAR WIRE

ROCHESTER ELECTRO-MEDICAL, INC.

Analytical scalp electrode, reusable Analytical scalp electrode, reusable Analytical scalp electrode, reusable Analytical scalp electrode, reusable Analytical scalp electrode, reusable Analytical scalp electrode, reusable Analytical scalp electrode, reusable Analytical scalp electrode, reusable Analytical scalp electrode, reusable Analytical scalp electrode, reusable Analytical scalp electrode, reusable

• Primary Device ID: 10816843020474
• NIH Device Record Key: ee795321-f692-41b8-870f-c2a775bf7d00
• Commercial Distribution Discontinuation: 2019-05-20
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: UltraLast™
• Version Model Number: BMS045T15-4
• Company DUNS: 068156330
• Company Name: ROCHESTER ELECTRO-MEDICAL, INC.
• Device Count: 10
• 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: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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: 18003285544
• Email: info@rochestermed.com
• Phone: 18003285544
• Email: info@rochestermed.com
• Phone: 18003285544
• Email: info@rochestermed.com
• Phone: 18003285544
• Email: info@rochestermed.com
• Phone: 18003285544
• Email: info@rochestermed.com
• Phone: 18003285544
• Email: info@rochestermed.com
• Phone: 18003285544
• Email: info@rochestermed.com
• Phone: 18003285544
• Email: info@rochestermed.com
• Phone: 18003285544
• Email: info@rochestermed.com
• Phone: 18003285544
• Email: info@rochestermed.com
• Phone: 18003285544
• Email: info@rochestermed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10816843020474 [Primary]
GS1	10816843020481 [Unit of Use]

FDA Product Code

• GXY: Electrode, Cutaneous

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2022-11-28
• Device Publish Date: 2016-09-24

On-Brand Devices [UltraLast™]

• 10816843024069: REUSABLE ULTRALAST CUP ELECTRODES: 6 MM STAMPED GOLD DISC, 6 FT. (1.8 M), SINGLE, KEVLAR WIRE
• 10816843020535: REUSABLE ULTRALAST CUP ELECTRODES: 9 MM MOLDED GOLD DISC, 8 FT. (2.5 M), SINGLE, KEVLAR WIRE
• 10816843020511: REUSABLE ULTRALAST CUP ELECTRODES: 9 MM MOLDED GOLD DISC, 6 FT. (1.8 M), SINGLE, KEVLAR WIRE
• 10816843020498: REUSABLE ULTRALAST CUP ELECTRODES: 9 MM MOLDED GOLD DISC, 5 FT. (1.5 M), SINGLE, KEVLAR WIRE
• 10816843020474: REUSABLE ULTRALAST CUP ELECTRODES: 9 MM MOLDED GOLD DISC, 4 FT. (1.2 M), SINGLE, KEVLAR WIRE
• 10816843020450: REUSABLE ULTRALAST CUP ELECTRODES: 9 MM MOLDED GOLD DISC, 10 FT. (3.1 M), SINGLE, KEVLAR WIRE
• 10816843020436: REUSABLE ULTRALAST CUP ELECTRODES: 9 MM MOLDED SILVER DISC, 6 FT. (1.8 M), SINGLE, KEVLAR WIRE
• 10816843020412: REUSABLE ULTRALAST CUP ELECTRODES: 9 MM MOLDED SILVER DISC, 5 FT. (1.5 M), SINGLE, KEVLAR WIRE
• 10816843020399: REUSABLE ULTRALAST CUP ELECTRODES: 9 MM MOLDED SILVER DISC, 4 FT. (1.2 M), SINGLE, KEVLAR WIRE