LED202X2

GUDID 00724995225094

LED202 IN CEILING DUAL LIGHTING SYSTEM

STERIS CORPORATION

Fixed examination/treatment room light

• Primary Device ID: 00724995225094
• NIH Device Record Key: 7c13940f-1802-44f1-beff-842eb04dd9aa
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: LED202
• Catalog Number: LED202X2
• Company DUNS: 036985604
• Company Name: STERIS CORPORATION
• 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: true

Customer Support Contacts

• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx
• Phone: +1(800)548-4873
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00724995225094 [Primary]

FDA Product Code

• KZF: Device, medical examination, ac 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: 2024-11-15
• Device Publish Date: 2024-11-07

Devices Manufactured by STERIS CORPORATION

• 00724995222017 - NA: 2024-12-03 Foot Extension with Siderail Locks, Velcro without Pad is used with the 7000 Series Surgical Table.
• 00724995222024 - NA: 2024-12-03 Foot Extension with Siderail Locks, Velcro with 2-inch TLT Pad is used with the 7000 Series Surgical Tables.
• 00724995222048 - NA: 2024-12-03 Bariatric Foot Extension withSiderail Locks, Velcro with 2-inch TLT Pad is used with the 7000 Series Surgical Table.
• 00724995222260 - NA: 2024-12-03 2-inch TLT Pad, Velcro, Foot Extension, is used with the 7000 Series Surgical Tables.
• 00724995222277 - NA: 2024-12-03 3-inch TLT Pad, Velcro, Foot Extension, is used with the 7000 Series Surgical Tables.
• 00724995222284 - NA: 2024-12-03 4-inch TLT Pad, Velcro, Foot Extension, is used with the 7000 Series Surgical Tables.
• 00724995222291 - NA: 2024-12-03 2-inch TLT Pad, Velcro, Bariatric Foot Extension, is used with the 7000 Series Surgical Tables.
• 00724995222307 - NA: 2024-12-03 3-inch TLT Pad, Velcro, Bariatric Foot Extension, is used with the 7000 Series Surgical Tables.