KENEX 313/A2/3.24

GUDID 05055449407762

313/A2/3.24 29cm Lift Off Top

KENEX (ELECTRO-MEDICAL) LIMITED

Radiation shielding curtain

• Primary Device ID: 05055449407762
• NIH Device Record Key: 0c23c396-fc8a-43cb-bc5f-f8b83be7d107
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KENEX
• Version Model Number: 313/A2/3.24
• Catalog Number: 313/A2/3.24
• Company DUNS: 217421064
• Company Name: KENEX (ELECTRO-MEDICAL) LIMITED
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	05055449407762 [Primary]

FDA Product Code

• KPY: Shield, Protective, Personnel

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: 2023-07-26
• Device Publish Date: 2023-07-18

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